Embodiments of the present invention generally relate to ultrasound treatment and imaging devices and more specifically relate to ultrasound devices having a transducer probe operable to emit and receive ultrasound energy for cosmetic treatment and imaging.
In general, a popular cosmetic procedure for reducing wrinkles on the brow region of a patient's face is a brow lift, during which portions of muscle, fat, fascia and other tissues in the brow region are invasively cut, removed, and/or paralyzed to help reduce or eliminate wrinkles from the brow. Traditionally, the brow lift requires an incision beginning at one ear and continuing around the forehead at the hair line to the other ear. A less invasive brow lift procedure is known as an endoscopic lift during which smaller incisions are made along the forehead and an endoscope and surgical cutting tools are inserted within the incisions to cut, remove, manipulate, or paralyze tissue to reduce or eliminate wrinkles from the brow.
Even less invasive cosmetic treatments are designed to inject a neurotoxin in the brow. This procedure paralyzes muscles within the brow which can assist in reducing wrinkles. However, such procedures are temporary, can require chronic usage to sustain the intended effects, and can have deleterious effects.
There is a need for non-invasive cosmetic procedures for reducing wrinkles in the head and neck, such as in a brow region, and in other regions. In addition, there is a need for non-invasive cosmetic procedures that result in a tightening of skin in the head and neck, including the brow region, and other regions. Further, there is a need to effectively and efficiently image the region of the skin that is targeted for treatment. In several of the embodiments described herein, the procedure is entirely cosmetic and not a medical act.
Accordingly, several embodiments of the present invention provide a system and method for cosmetic treatment and imaging. In various embodiments the treatment system includes a hand wand with at least one finger activated control, or controller, and a removable transducer module having at least one ultrasound transducer. In one embodiment, the system includes a control module that is coupled to the hand wand and has a graphic user interface for controlling the removable transducer module that has an interface coupling the hand wand to the control module. In an aspect of the embodiment, the interface provides power to the hand wand and/or transfers a signal from the hand wand to the control module. In various embodiments of the present invention, the cosmetic treatment and imaging system is used in aesthetic procedures on a portion of a head of patient, including the face, scalp, neck and/or ears of a patient.
In accordance with one embodiment of an aesthetic imaging system, the aesthetic imaging system includes a hand wand, a removable transducer module, a control module, and an interface coupling the hand wand and the control module. The hand wand includes at least one finger activated controller. The removable transducer module includes an ultrasound transducer and at least one interface coupleable to the hand wand. The control module is coupled to the hand wand and includes a graphical user interface for controlling the removable transducer module. In one embodiment, the interface couples the hand wand to the control module, and provides at least power to the hand wand. In one embodiment, the interface transfers one or more signals between the hand wand and the control module. In one embodiment, at least one signal (e.g., 1, 2, 3, 4, 5 or more signals) is communicated from the wand to the control module. In another embodiment, at least one signal (e.g., 1, 2, 3, 4, 5 or more signals) is communicated from the control module to the wand. In several embodiments, at least one signal (e.g., 1, 2, 3, 4, 5 or more signals) is communicated to, from, or between the wand and control module. In one embodiment, the aesthetic imaging system also includes a printer coupled to the control module and the control module provides an output signal and power to the printer. In one embodiment, the aesthetic imaging system also includes a key operable to unlock the control module for controlling the removable transducer module. In one embodiment of an aesthetic imaging system, the hand wand includes a movement mechanism, operable to move the ultrasound transducer within the transducer module. In one embodiment, the aesthetic imaging system also includes at least one sensor coupled to the hand wand and/or the removable transducer module.
In accordance with one embodiment of a hand wand for use in cosmetic treatment, the wand includes a first controlling device operably controlling an imaging function, a second controlling device operably controlling a treatment function, a status indicator, an input for power, an output for at least one signal, a movement mechanism and a removable transducer module operably coupled to at least one of the first controlling device, the second controlling device and the movement mechanism. In one embodiment, the hand wand includes a latch mechanism removably holding the transducer module in the wand. In one embodiment, the hand wand includes a cable for communicating at least one of the input and the output. In one embodiment, the hand wand includes a controller operably interfacing with a cable, where the controller has a graphical user interface for controlling the removable transducer module. In one embodiment, the hand wand includes a first transducer module coupled to the first controlling device and a second transducer module coupled to the second controlling device.
In accordance with one embodiment of a device for cosmetic imaging and treatment, the device includes a removable transducer module and a controller. In one embodiment, the transducer module is not removable. In one embodiment, the transducer module is integrated, or permanently attached. The removable transducer module is interfaced to a hand enclosure having at least one controller button such that the transducer module and button is operable using one hand. The transducer module provides ultrasound energy for at least one of an imaging function and a treatment function. The controller is coupled to the hand enclosure and is interfaced to the transducer module. The controller controls the ultrasound energy and receives at least one signal from the transducer module. The controller has a power supply operably providing power for at least the ultrasound energy. In one embodiment, the device also includes a graphical user interface for controlling the transducer module and for viewing the at least one signal from the transducer module. In one embodiment, the device has a hand enclosure that also includes a movement mechanism operably moving a transducer in the transducer module, where the movement mechanism is controlled by the controller. In one embodiment, the device has at least one controller button as a first controller button controlling the imaging function and a second controlling button controlling the treatment function. In various embodiments, the device has a treatment function that is one of face lift, a brow lift, a chin lift, a wrinkle reduction, a scar reduction, a tattoo removal, a vein removal, sun spot removal, and pimple removal. In another embodiment the device may be used on adipose tissue.
In accordance with one embodiment of a method of performing cosmetic treatment on a facial (or other) area of a subject, the method includes inserting a transducer module into a hand controller, coupling the transducer module to the subject, activating a first switch on the hand controller operably initiating an imaging sequence of a portion of tissue below the dermal layer, collecting data from the imaging sequence, calculating a treatment sequence from the data, and activating a second switch on the hand controller operably initiating the treatment sequence. In one embodiment, the method also includes emitting a first ultrasound energy from a first transducer in the transducer module operably providing a source for the imaging sequence. In one embodiment, the method also includes emitting a second ultrasound energy from a second transducer in the transducer module operably providing a source for the treatment sequence. In one embodiment, the method also includes tightening a portion of the dermal layer on a facial area of a subject. In one embodiment, the method provides for the transducer module to permit the treatment sequence at a fixed depth below the dermal layer.
In accordance with one embodiment of a hand wand for use in cosmetic treatment, the wand includes a first controlling device operably controlling an ultrasonic imaging function, a second controlling device operably controlling an ultrasonic treatment function, a movement mechanism configured for travel through a liquid-tight seal, and a fluid-filled transducer module. In one embodiment, the fluid-filled transducer module is operably coupled to at least one of the first controlling, the second controlling device and the movement mechanism. In one embodiment, the fluid-filled transducer module is mechanically and electrically separable from at least one of the first controlling, the second controlling device and the movement mechanism. In one embodiment, the fluid-filled transducer module includes an acoustic liquid. In one embodiment, the fluid-filled transducer module includes a gel adapted to enhance transmission of an ultrasonic signal. In one embodiment, a gel adapted to enhance transmission of an ultrasonic signal is placed between the transducer and the patient's skin.
In accordance with one embodiment of a hand wand for use in cosmetic treatment, the wand includes a first controlling device operably controlling an ultrasonic imaging function, a second controlling device operably controlling an ultrasonic treatment function, and a movement mechanism configured to create a linear sequence of individual thermal lesions with the second controlling device. In one embodiment, the movement mechanism is configured to be automated and programmable by a user. In one embodiment, the wand includes a transducer module operably coupled to at least one of the first controlling device, the second controlling device and the movement mechanism. In one embodiment, the linear sequence of individual thermal lesions has a treatment spacing in a range from about 0.01 mm to about 25 mm. In one embodiment, the movement mechanism is configured to be programmed to provide variable spacing between the individual thermal lesions. In one embodiment the individual thermal lesions are discrete. In one embodiment the individual thermal lesions are overlapping.
In accordance with one embodiment of a variable ultrasonic parameter ultrasonic system for use in cosmetic treatment, the system includes a first controlling device, a second controlling device, a movement mechanism, and one or more removable transducer modules. In various embodiments, the one or more removable transducer modules includes two, three, four, five, six, or more removable transducer modules. In various embodiments, the different numbers of removable transducer modules can be configured for different or variable ultrasonic parameters. For example, in various non-limiting embodiments, the ultrasonic parameter can relate to transducer geometry, size, timing, spatial configuration, frequency, variations in spatial parameters, variations in temporal parameters, coagulation formation, depth, width, absorption coefficient, refraction coefficient, tissue depths, and/or other tissue characteristics. In various embodiments, a variable ultrasonic parameter may be altered, or varied, in order to effect the formation of a lesion for the desired cosmetic approach. In various embodiments, a variable ultrasonic parameter may be altered, or varied, in order to effect the formation of a lesion for the desired clinical approach. By way of example, one variable ultrasonic parameter relates to aspects of configurations associated with tissue depth. For example, some non-limiting embodiments of removable transducer modules can be configured for a tissue depth of 3 mm, 4.5 mm, 6 mm, less than 3 mm, between 3 mm and 4.5 mm, more than more than 4.5 mm, more than 6 mm, and anywhere in the ranges of 0-3 mm, 0-4.5 mm, 0-25 mm, 0-100 mm, and any depths therein. In one embodiment, an ultrasonic system is provided with two transducer modules, in which the first module applies treatment at a depth of about 4.5 mm and the second module applies treatment at a depth of about 3 mm. An optional third module that applies treatment at a depth of about 1.5-2 mm is also provided. A combination of two or more treatment modules is particularly advantageous because it permits treatment of a patient at varied tissue depths, thus providing synergistic results and maximizing the clinical results of a single treatment session. For example, treatment at multiple depths under a single surface region permits a larger overall volume of tissue treatment, which results in enhanced collagen formation and tightening. Additionally, treatment at different depths affects different types of tissue, thereby producing different clinical effects that together provide an enhanced overall cosmetic result. For example, superficial treatment may reduce the visibility of wrinkles and deeper treatment may induce formation of more collagen growth.
Although treatment of a subject at different depths in one session may be advantageous in some embodiments, sequential treatment over time may be beneficial in other embodiments. For example, a subject may be treated under the same surface region at one depth in week 1, a second depth in week 2, etc. The new collagen produced by the first treatment may be more sensitive to subsequent treatments, which may be desired for some indications. Alternatively, multiple depth treatment under the same surface region in a single session may be advantageous because treatment at one depth may synergistically enhance or supplement treatment at another depth (due to, for example, enhanced blood flow, stimulation of growth factors, hormonal stimulation, etc.).
In several embodiments, different transducer modules provide treatment at different depths. In several embodiments, a system comprising different transducers, each having a different depth, is particularly advantageous because it reduces the risk that a user will inadvertently select an incorrect depth. In one embodiment, a single transducer module can be adjusted or controlled for varied depths. Safety features to minimize the risk that an incorrect depth will be selected can be used in conjunction with the single module system.
In several embodiments, a method of treating the lower face and neck area (e.g., the submental area) is provided. In several embodiments, a method of treating (e.g., softening) mentolabial folds is provided. In other embodiments, a method of treating the eye region is provided. Upper lid laxity improvement and periorbital lines and texture improvement will be achieved by several embodiments by treating at variable depths. In one embodiment, a subject is treated with about 40-50 lines at depths of 4.5 and 3 mm. The subject is optionally treated with about 40-50 lines at a depth of about 1.5-2 mm. The subject is optionally treated with about 40-50 lines at a depth of about 6 mm. By treating at varied depths in a single treatment session, optimal clinical effects (e.g., softening, tightening) can be achieved.
In several embodiments, the treatment methods described herein are non-invasive cosmetic procedures. In some embodiments, the methods can be used in conjunction with invasive procedures, such as surgical facelifts or liposuction, where skin tightening is desired.
In accordance with one embodiment of a variable ultrasonic parameter system for use in cosmetic treatment, the system includes a first controlling device, a second controlling device, a movement mechanism, a first removable transducer module and a second removable transducer module. The first controlling device operably controls an ultrasonic imaging function. The second controlling device operably controls an ultrasonic treatment function. The movement mechanism is configured to create a linear sequence of individual thermal lesions for treatment purposes. The first removable transducer module is configured to treat tissue at a first tissue depth. The second removable transducer module is configured to treat tissue at a second tissue depth. The first and second transducer modules are interchangeably coupled to a hand wand. The first and second transducer modules are operably coupled to at least one of the first controlling device, the second controlling device and the movement mechanism. Rapid interchangeability and exchange of multiple modules on a single unit facilitates treatment in several embodiments. In one embodiment the individual thermal lesions are discrete. In one embodiment the individual thermal lesions are overlapping, merged, etc.
In accordance with one embodiment of an aesthetic imaging and treatment system includes a hand wand, a removable transducer module, a control module and an interface coupling the hand wand to the control module. The hand wand includes at least one finger activated controller. The removable transducer module includes an ultrasound transducer and at least one interface coupleable to the hand wand. The control module is coupled to the hand wand and includes a graphical user interface for controlling the removable transducer module. The interface coupling the hand wand to the control module transfers at least a signal between the hand wand and the control module. In one embodiment, the system also includes a printer coupled to the control module, with the control module providing an output signal and power to the printer. In one embodiment, the system also includes a key operable to unlock the control module for controlling the removable transducer module. In one embodiment, the hand wand also includes a movement mechanism, the movement mechanism operable to move the ultrasound transducer within the transducer module. In one embodiment, the system also includes at least one sensor coupled to one of the hand wand and the removable transducer module.
In accordance with one embodiment of a hand wand for use in cosmetic treatment, the wand includes a first controlling device operably controlling an imaging function, a second controlling device operably controlling a treatment function, a status indicator, an input for power, an output for at least one signal, a movement mechanism, and a removable transducer module operably coupled to at least one of the first controlling device, the second controlling device and the movement mechanism. In one embodiment, the system also includes a latch mechanism removably holding the transducer module in the wand. In one embodiment, the system also includes a cable for communicating at least one of the input and the output. In one embodiment, the system also includes a controller operably interfacing with the cable, the controller having a graphical user interface for controlling the removable transducer module. In one embodiment, the transducer module has a first transducer coupled to the first controlling device and a second transducer coupled to the second controlling device.
In accordance with one embodiment of a device for cosmetic treatment, the device includes a removable transducer module interfaced to a hand enclosure and a controller coupled to the hand enclosure and interfaced to the transducer module. The removable transducer module has at least one controller button such that the transducer module and button are operable using one hand. The transducer module provides ultrasound energy for a treatment function. The controller controls the ultrasound energy and receives at least one signal from the transducer module. The controller has a power supply operably providing power for at least the ultrasound energy. In one embodiment, the controller also includes a graphical user interface for controlling the transducer module and for viewing the at least one signal from the transducer. In one embodiment, the hand enclosure also includes a movement mechanism operably moving a transducer in the transducer module, the movement mechanism being controlled by the controller. In one embodiment, the at least one controller button includes a first controller button controlling the imaging function and a second controlling button controlling the treatment function. In one embodiment, the treatment function is at least one of face lift, a brow lift, a chin lift, a wrinkle reduction, a scar reduction, a tattoo removal, a vein removal, sun spot removal, and acne treatment
In accordance with one embodiment of a method of performing cosmetic treatment a facial area of a subject, the method includes inserting a transducer module into a hand controller, coupling the transducer module to the facial area of the subject, activating a first switch on the hand controller operably initiating an imaging sequence of a portion of tissue below the dermal layer, collecting data from the imaging sequence, calculating a treatment sequence from the data, and activating a second switch on the hand controller operably initiating the treatment sequence. In one embodiment, the method also includes emitting a first ultrasound energy from a first transducer in the transducer module operably providing a source for the imaging sequence. In one embodiment, the method also includes emitting a second ultrasound energy from a second transducer in the transducer module operably providing a source for the treatment sequence. In one embodiment, the method also includes tightening a portion of the dermal layer on a facial area of a subject. In one embodiment, the transducer module permits the treatment sequence at a fixed depth below the dermal layer.
In several embodiments, the invention comprises a hand wand for use in cosmetic treatment. In one embodiment, the wand comprises a first controlling device operably controlling an ultrasonic imaging function for providing ultrasonic imaging and a second controlling device operably controlling an ultrasonic treatment function for providing ultrasonic treatment. The controlling devices, in some embodiments, are finger/thumb operated buttons or keys that communicate with a computer processor. The wand also comprises a movement mechanism configured to direct ultrasonic treatment in a linear sequence of individual thermal lesions. In one embodiment, the linear sequence of individual thermal lesions has a treatment spacing in a range from about 0.01 mm to about 25 mm. In one embodiment the individual thermal lesions are discrete. In one embodiment the individual thermal lesions are overlapping. The movement mechanism is configured to be programmed to provide variable spacing between the individual thermal lesions. First and second removable transducer modules are also provided. Each of the first and second transducer modules are configured for both ultrasonic imaging and ultrasonic treatment. The first and second transducer modules are configured for interchangeable coupling to the hand wand. The first transducer module is configured to apply ultrasonic therapy to a first layer of tissue, while the second transducer module is configured to apply ultrasonic therapy to a second layer of tissue. The second layer of tissue is at a different depth than the first layer of tissue. The first and second transducer modules are configured to be operably coupled to at least one of the first controlling device, the second controlling device and the movement mechanism.
In one embodiment, a third transducer module is provided. The third transducer module is configured to apply ultrasonic therapy to a third layer of tissue, wherein the third layer of tissue is at a different depth than the first or second layers of tissue. Fourth and fifth modules are provided in additional embodiments. The transducer modules are configured to provide variable depth treatment and the movement mechanism is configured to provide variable treatment along a single depth level.
In one embodiment, at least one of the first controlling device and the second controlling device is activated by a control. The control module comprises a processor and a graphical user interface for controlling the first and second transducer modules.
A method of performing a cosmetic procedure on a subject using a hand wand as described herein is provided in several embodiments. In one embodiment, the method comprises ultrasonically imaging a first target region on the subject with the first transducer module and ultrasonically treating the first target region on the subject with the first transducer module at the first tissue depth. The treatment comprises multiple treatment lines across the first target region that are automatically selected (e.g., programmed, pre-set, etc.) by the movement mechanism. In one embodiment, the method further comprises exchanging the first transducer module with the second transducer module; ultrasonically imaging a second target region on the subject with the second transducer module; and ultrasonically treating the second target region on the subject with the second transducer module at the second tissue depth. The treatment comprises multiple treatment lines across the second target region that are automatically selected (e.g., programmed, pre-set, etc.) by the movement mechanism. In one embodiment, the first and second target regions are located under a single surface of the subject.
In several embodiments, the invention comprises a hand wand for use in cosmetic treatment. In accordance with one embodiment, the hand wand comprises a first controlling device, a second controlling device, a movement mechanism, and a transducer module. The first controlling device operably controls an ultrasonic imaging function for providing ultrasonic imaging. The second controlling device operably controls an ultrasonic treatment function for providing ultrasonic treatment. The movement mechanism is configured to direct ultrasonic treatment in a sequence of individual thermal lesions. The removable transducer module is configured for both ultrasonic imaging and ultrasonic treatment. The removable transducer module is configured for interchangeable coupling to the hand wand. The removable transducer module is configured to be operably coupled to at least one of said first controlling device, said second controlling device and said movement mechanism. The removable transducer module is configured to apply ultrasonic therapy to at a first variable ultrasonic parameter to tissue.
In one embodiment, the hand wand is configured to apply ultrasonic therapy to at a second variable ultrasonic parameter to tissue. In one embodiment, the removable transducer module is configured to apply ultrasonic therapy to at a second variable ultrasonic parameter to tissue. In one embodiment, the hand wand further comprises a second removable transducer module, wherein the second removable transducer module is configured to apply ultrasonic therapy to at the second variable ultrasonic parameter to tissue. In one embodiment, the variable ultrasonic parameter is tissue depth. In one embodiment, the variable ultrasonic parameter is frequency. In one embodiment, the variable ultrasonic parameter is timing. In one embodiment, the variable ultrasonic parameter is geometry.
In several embodiments, the invention comprises a hand wand for use in cosmetic treatment. In one embodiment, the wand comprises at least one controlling device, movement mechanism and transducer module. In one embodiment, the wand comprises at least one controlling device operably controlling an ultrasonic imaging function for providing ultrasonic imaging and operably controlling an ultrasonic treatment function for providing ultrasonic treatment. One, two or more controlling devices may be used. A movement mechanism configured to direct ultrasonic treatment in a sequence of individual thermal lesions is provided. The transducer module is configured for both ultrasonic imaging and ultrasonic treatment and is operably coupled to at least one controlling device and a movement mechanism. The transducer module is configured to apply ultrasonic therapy at a first ultrasonic parameter and a second ultrasonic parameter. In various embodiments, the first and second ultrasonic parameters are selected from the group consisting of: variable depth, variable frequency, and variable geometry. For example, in one embodiment, a single transducer module delivers ultrasonic therapy at two or more depths. In another embodiment, two or more interchangeable transducer modules each provide a different depth (e.g., one module treats at 3 mm depth while the other treats at a 4.5 mm depth). In yet another embodiment, a single transducer module delivers ultrasonic therapy at two or more frequencies, geometries, amplitudes, velocities, wave types, and/or wavelengths. In other embodiments, two or more interchangeable transducer modules each provide a different parameter value. In one embodiment, a single transducer may provide at least two different depths and at least two different frequencies (or other parameter). Variable parameter options are particularly advantageous in certain embodiments because they offer enhanced control of tissue treatment and optimize lesion formation, tissue coagulation, treatment volume, etc.
Further areas of applicability will become apparent from the description provided herein. It should be understood that the description and specific examples are intended for purposes of illustration only and are not intended to limit the scope of the embodiments disclosed herein.
The drawings described herein are for illustration purposes only and are not intended to limit the scope of the present disclosure in any way. Embodiments of the present invention will become more fully understood from the detailed description and the accompanying drawings wherein:
The following description sets forth examples of embodiments, and is not intended to limit the present invention or its teachings, applications, or uses thereof. It should be understood that throughout the drawings, corresponding reference numerals indicate like or corresponding parts and features. The description of specific examples indicated in various embodiments of the present invention are intended for purposes of illustration only and are not intended to limit the scope of the invention disclosed herein. Moreover, recitation of multiple embodiments having stated features is not intended to exclude other embodiments having additional features or other embodiments incorporating different combinations of the stated features. Further, features in one embodiment (such as in one figure) may be combined with descriptions (and figures) of other embodiments.
In accordance with on embodiment of the present invention, methods and systems for ultrasound treatment of tissue are configured to provide cosmetic treatment. In various embodiments of the present invention, tissue below or even at a skin surface such as epidermis, dermis, fascia, and superficial muscular aponeurotic system (“SMAS”), are treated non-invasively with ultrasound energy. The ultrasound energy can be focused, unfocused or defocused and applied to a region of interest containing at least one of epidermis, dermis, hypodermis, fascia, and SMAS to achieve a therapeutic effect. In one embodiment, the present invention provides non-invasive dermatological treatment to produce eyebrow lift through tissue coagulation and tightening. In one embodiment, the present invention provides imaging of skin and sub-dermal tissue. Ultrasound energy can be focused, unfocused or defocused, and applied to any desired region of interest, including adipose tissue. In one embodiment, adipose tissue is specifically targeted.
In various embodiments of the present invention, certain cosmetic procedures that are traditionally performed through invasive techniques are accomplished by targeting energy, such as ultrasound energy, at specific subcutaneous tissues. In several embodiments, methods and systems for non-invasively treating subcutaneous tissues to perform a brow lift are provided; however, various other cosmetic treatment applications, such as face lifts, acne treatment and/or any other cosmetic treatment application, can also be performed with the cosmetic treatment system. In one embodiment, a system integrates the capabilities of high resolution ultrasound imaging with that of ultrasound therapy, providing an imaging feature that allows the user to visualize the skin and sub-dermal regions of interest before treatment. In one embodiment, the system allows the user to place a transducer module at optimal locations on the skin and provides feedback information to assure proper skin contact. In one embodiment, the therapeutic system provides an ultrasonic transducer module that directs acoustic waves to the treatment area. This acoustic energy heats tissue as a result of frictional losses during energy absorption, producing a discrete zone of coagulation.
In various embodiments, the device includes a removable transducer module interfaced to a hand enclosure having at least one controller button such that the transducer module and the controller button is operable using only one hand. In an aspect of the embodiments, the transducer module provides ultrasound energy for an imaging function and/or a treatment function. In another aspect of the embodiments, the device includes a controller coupled to the hand-held enclosure and interfaced to the transducer module. In a further aspect of the embodiments, the controller controls the ultrasound energy and receives a signal from the transducer module. The controller can have a power supply and driver circuits providing power for the ultrasound energy. In still another aspect of the embodiments, the device is used in cosmetic imaging and treatment of a patient, or simply treatment of the patient, such as on a brow of a patient.
In accordance with one embodiment for a method of performing a brow lift on a patient, the method includes coupling a probe to a brow region of the patient and imaging at least a portion of subcutaneous tissue of the brow region to determine a target area in the subcutaneous tissue. In one embodiment, the method includes administering ultrasound energy into the target area in the subcutaneous tissue to ablate or coagulate the subcutaneous tissue in the target area, which causes tightening of a dermal layer above or below the subcutaneous tissue of the brow region.
Moreover, several embodiments of the present invention provide a method of tightening a portion of a dermal layer on a facial area of a patient. In various embodiments, the method includes inserting a transducer module into a hand controller and then coupling the transducer module to a facial area of the patient. In one embodiment, the method includes activating a first switch on the hand to initiate an imaging sequence of a portion of tissue below a dermal layer, then collecting data from the imaging sequence. In these embodiments, the method includes calculating a treatment sequence from the collected data, and then activating a second switch on the hand to initiate the treatment sequence. In an aspect of the embodiments, the method can be useful on a portion of a face, head, neck and/or other part of the body of a patient.
In some embodiments, the system includes a hand wand with at least one finger activated controller, and a removable transducer module having an ultrasound transducer. In one embodiment, the system includes a control module that is coupled to the hand wand and has a graphic user interface for controlling the removable transducer module with an interface coupling the hand wand to the control module. In one embodiment, the interface provides power to the hand wand. In one embodiment, the interface transfers at least one signal between the hand wand and the control module. In one embodiment, the aesthetic imaging system is used in cosmetic procedures on a portion of a face, head, neck and/or other part of the body of a patient.
In addition, several embodiments of the present invention provide a hand wand for use in aesthetic treatment. In some embodiments, the hand wand includes a first controlling device operably controlling an imaging function, a second controlling device operably controlling a treatment function, a status indicator, an input for power, an output for at least one signal, and a movement mechanism. A removable transducer module can be coupled to the hand wand. The removable transducer module can be interfaced with the first controlling device, the second controlling device and/or the movement mechanism. In one embodiment, the hand wand is used in cosmetic procedures on a face, head, neck and/or other part of the body of a patient.
Several embodiments of the present invention may be described herein in terms of various components and processing steps. It should be appreciated that such components and steps may be realized by any number of hardware components configured to perform the specified functions. For example, some embodiments of the present invention may employ various medical treatment devices, visual imaging and display devices, input terminals and the like, which may carry out a variety of functions under the control of one or more control systems or other control devices. Several embodiments of the present invention may be practiced in any number of medical contexts. For example, the principles, features and methods discussed may be applied to any medical application.
To further explain in more detail various aspects of embodiments of the present invention, several examples of a cosmetic treatment system as used with a control system and an ultrasonic probe system will be provided. However, it should be noted that the following embodiments are for illustrative purposes, and that embodiments of the present invention can comprise various other configurations for a cosmetic treatment. In addition, although not illustrated in the drawing figures, the cosmetic treatment system can further include components associated with imaging, diagnostic, and/or treatment systems, such as any required power sources, system control electronics, electronic connections, and/or additional memory locations.
With reference to the illustration in
In various embodiments, the controller 300 can be configured for operation with the hand wand 100 and the emitter-receiver module 200, as well as the overall CTS 20 functionality. In various embodiments, multiple controllers 300, 300′, 300″, etc. can be configured for operation with multiple hand wands 100, 100′, 100″, etc. and or multiple emitter-receiver modules 200, 200′, 200″, etc. In various embodiments, a second embodiment of a reference can be indicated with a reference number with one or more primes (′). For example, in one embodiment a first module 200 may be used with or as an alternative to a second module 200′, third module 200″, fourth module 200′″, etc. Likewise, in various embodiments, any part with multiples can have a reference number with one or more primes attached to the reference number in order to indicate that embodiment. For example, in one embodiment a first transducer 280 can be indicated with the 280 reference number, and a second transducer 280′ uses the prime. In one embodiment, controller 300 houses an interactive graphical display 310, which can include a touch screen monitor and Graphic User Interface (GUI) that allows the user to interact with the CTS 20. In various embodiments, this display 310 sets and displays the operating conditions, including equipment activation status, treatment parameters, system messages and prompts and ultrasound images. In various embodiments, the controller 300 can be configured to include, for example, a microprocessor with software and input/output devices, systems and devices for controlling electronic and/or mechanical scanning and/or multiplexing of transducers and/or multiplexing of transducer modules, a system for power delivery, systems for monitoring, systems for sensing the spatial position of the probe and/or transducers and/or multiplexing of transducer modules, and/or systems for handling user input and recording treatment results, among others. In various embodiments, the controller 300 can comprise a system processor and various digital control logic, such as one or more of microcontrollers, microprocessors, field-programmable gate arrays, computer boards, and associated components, including firmware and control software, which may be capable of interfacing with user controls and interfacing circuits as well as input/output circuits and systems for communications, displays, interfacing, storage, documentation, and other useful functions. System software may be capable of controlling all initialization, timing, level setting, monitoring, safety monitoring, and all other system functions required to accomplish user-defined treatment objectives. Further, the controller 300 can include various control switches that may also be suitably configured to control operation of the CTS 20. In one embodiment, the controller 300 includes an interactive graphical display 310 for conveying information to user. In one embodiment, the controller 300 includes one or more data ports 390. In one embodiment, the data port 390 is a USB port, and can be located on the front, side, and/or back of the controller 300 for access to storage, a printer 391, devices, or be used for other purposes. In various embodiments the CTS 20 includes a lock 395, and in one embodiment the lock 395 can be connectable to the controller 300 via a USB port. In one embodiment, in order to operate CTS 20, lock 395 must be unlocked so that power switch 393 may be activated. In another embodiment lock 395 must be unlocked insertion of USB access key or hardware dongle and associated software so that the interactive graphical display 310 can execute. In one embodiment, an emergency stop button 392 is readily accessible for emergency de-activation.
In various embodiments, an aesthetic imaging system or CTS 20 includes a hand wand 100 with at least one finger activated controller (150 and/or 160), and a removable emitter-receiver module 200 having an ultrasound transducer. Other embodiments may include non-removable emitter-receiver modules, imaging-only emitter-receiver modules, treatment-only emitter-receiver modules, and imaging-and-treatment emitter-receiver modules. In one embodiment, the CTS 20 includes a control module 300 that is coupled to the hand wand 100 and has a graphic user interface 310 for controlling the removable transducer module 200 with an interface 130, such as in one embodiment, a cord coupling the hand wand 100 to the control module 300. In one embodiment, the interface 130 provides power to the hand wand 100. In one embodiment, the interface 130 transfers at least one signal between the hand wand 100 and the control module 300. In an aspect of this embodiment, the aesthetic imaging system of CTS 20 is used in aesthetic procedures on a portion of a head of a patient. In one embodiment, the CTS 20 is used in aesthetic procedures on a portion of a face, head, neck and/or other part of the body of a patient.
In addition, certain embodiments of the present invention provide a hand wand 100 for use in aesthetic treatment. In some embodiments, the hand wand 100 includes a first controlling device 150 operably controlling an imaging function, a second controlling device 160 operably controlling a treatment function, a status indicator 155, an input for power, an output for at least one signal (for example to a controller 300), a movement mechanism 400, and a removable transducer module 200 in communication with the first controlling device 150, the second controlling device 160 and/or the movement mechanism 400. In an aspect of the embodiments, the hand wand 100 is used in cosmetic procedures on a face, head, neck and/or other part of the body of a patient.
In accordance to various embodiments of the present invention, an emitter-receiver module 200 can be coupled to the hand wand 100. In some embodiments an emitter-receiver module 200 can emit and receive energy, such as ultrasonic energy. In one embodiment, an emitter-receiver module 200 can be configured to only emit energy, such as ultrasonic energy. In one embodiment, the emitter-receiver module 200 is permanently attachable to the hand wand 100. In one embodiment, the emitter-receiver module 200 is attachable to and detachable from the hand wand 100. The emitter-receiver module 200 can be mechanically coupled to the hand wand 100 using a latch or coupler 140. An interface guide 235 can be useful in assisting the coupling of the emitter-receiver module 200 to the hand wand 100. In addition, the emitter-receiver module 200 can be electronically coupled to the hand wand 100 and such coupling may include an interface which is in communication with the controller 300. In one embodiment, an electric coupler at the interface guide 235, located at a proximal end of an emitter-receiver module 200 provides for electronic communication between the emitter-receiver module 200 and the hand wand 100, which can both be in electric communication with a controller 300. The emitter-receiver module 200 can comprise various probe and/or transducer configurations. For example, the emitter-receiver module 200 can be configured for a combined dual-mode imaging/therapy transducer, coupled or co-housed imaging/therapy transducers, or simply a separate therapy probe and an imaging probe. In one embodiment, the hand wand 100 includes a handle with an integrated receptacle for insertion of an emitter-receiver module 200 containing at least a transducer on one end and an electrical cable for attachment to the controller 200 on the other end.
With additional reference to the illustrations in
In one embodiment, the emitter-receiver module 200 is configured to removably attach both electronically and mechanically with a hand wand 100. In one embodiment, a motion mechanism 400 (see
In various embodiments, the transducer 280 is in communication with the controller 300. In one embodiment, the transducer 280 is electronically coupled to the hand wand 100 and/or the controller 300. In one embodiment, the housing 220 is sealed by the cap 222 and the structure of the combination of the housing 220 and the cap 222 can hold a liquid (not shown). As illustrated in
In various embodiments, as illustrated in the block diagram of
In one embodiment, one or more sensors 201 may be included in the emitter-receiver module 200. In one embodiment, one or more sensors 201 may be included in the emitter-receiver module 200 to ensure that a mechanical coupling between the movement member 432 and the transducer holder 289 is indeed coupled. In one embodiment, an encoder 283 may be positioned on top of the transducer holder 289 and a sensor 201 may be located in a dry portion of the emitter-receiver module 200, or vice versa (swapped). In various embodiments the sensor 201 is a magnetic sensor, such as a giant magnetoresistive effect (GMR) or Hall Effect sensor, and the encoder a magnet, collection of magnets, or multi-pole magnetic strip. The sensor may be positioned as a transducer module home position. In one embodiment, the sensor 201 is a contact pressure sensor. In one embodiment, the sensor 201 is a contact pressure sensor on a surface of the device to sense the position of the device or the transducer on the patient. In various embodiments, the sensor 201 can be used to map the position of the device or a component in the device in one, two, or threes dimensions. In one embodiment the sensor 201 is configured to sense the position, angle, tilt, orientation, placement, elevation, or other relationship between the device (or a component therein) and the patient. In one embodiment, the sensor 201 comprises an optical sensor. In one embodiment, the sensor 201 comprises a roller ball sensor. In one embodiment, the sensor 201 is configured to map a position in one, two and/or three dimensions to compute a distance between areas or lines of treatment on the skin or tissue on a patient. Motion mechanism 400 can be any motion mechanism that may be found to be useful for movement of the transducer 280. Other embodiments of motion mechanisms useful herein can include worm gears and the like. In various embodiments of the present invention, the motion mechanism is located in the emitter-receiver module 200. In various embodiments, the motion mechanism can provide for linear, rotational, multi-dimensional motion or actuation, and the motion can include any collection of points and/or orientations in space. Various embodiments for motion can be used in accordance with several embodiments, including but not limited to rectilinear, circular, elliptical, arc-like, spiral, a collection of one or more points in space, or any other 1-D, 2-D, or 3-D positional and attitudinal motional embodiments. The speed of the motion mechanism 400 may be fixed or may be adjustably controlled by a user. One embodiment, a speed of the motion mechanism 400 for an image sequence may be different than that for a treatment sequence. In one embodiment, the speed of the motion mechanism 400 is controllable by the controller 300.
Transducer 280 can have a travel distance 272 such that an emitted energy 50 is able to be emitted through the acoustically transparent member 230. In one embodiment, the travel 272 is described as end-to-end range of travel of the transducer 280. In one embodiment, the travel 272 of the transducer 280 can be between about 100 mm and about 1 mm. In one embodiment, the length of the travel 272 can be about 25 mm. In one embodiment, the length of the travel 272 can be about 15 mm. In one embodiment, the length of the travel 272 can be about 10 mm. In various embodiments the length of the travel 272 can be about between 0-25 mm, 0-15 mm, 0-10 mm.
The transducer 280 can have an offset distance 270, which is the distance between the transducer 280 and the acoustically transparent member 230. In various embodiments of the present invention, the transducer 280 can image and treat a region of interest of about 25 mm and can image a depth less than about 10 mm. In one embodiment, the emitter-receiver module 200 has an offset distance 270 for a treatment at a depth 278 of about 4.5 mm below the skin surface 501 (see
In various embodiments, transducer modules 200 can be configured for different or variable ultrasonic parameters. For example, in various non-limiting embodiments, the ultrasonic parameter can relate to aspects of the transducer 280, such as geometry, size, timing, spatial configuration, frequency, variations in spatial parameters, variations in temporal parameters, coagulation formation, depth, width, absorption coefficient, refraction coefficient, tissue depths, and/or other tissue characteristics. In various embodiments, a variable ultrasonic parameter may be altered, or varied, in order to effect the formation of a lesion for the desired cosmetic approach. In various embodiments, a variable ultrasonic parameter may be altered, or varied, in order to effect the formation of a lesion for the desired clinical approach. By way of example, one variable ultrasonic parameter relates to configurations associated with tissue depth 278. In several embodiments, the transducer module 200 is configured for both ultrasonic imaging and ultrasonic treatment and is operably coupled to at least one controlling device 150, 160 and a movement mechanism 400. The transducer module 200 is configured to apply ultrasonic therapy at a first ultrasonic parameter and a second ultrasonic parameter. In various embodiments, the first and second ultrasonic parameters are selected from the group consisting of: variable depth, variable frequency, and variable geometry. For example, in one embodiment, a single transducer module 200 delivers ultrasonic therapy at two or more depths 278, 278′. In another embodiment, two or more interchangeable transducer modules 200 each provide a different depth 278 (e.g., one module treats at 3 mm depth while the other treats at a 4.5 mm depth). In yet another embodiment, a single transducer module 200 delivers ultrasonic therapy at two or more frequencies, geometries, amplitudes, velocities, wave types, and/or wavelengths. In other embodiments, two or more interchangeable transducer modules 200 each provide a different parameter value. In one embodiment, a single transducer module 200 may provide at least two different depths 278, 278′ and at least two different frequencies (or other parameter). Variable parameter options are particularly advantageous in certain embodiments because they offer enhanced control of tissue treatment and optimize lesion formation, tissue coagulation, treatment volume, etc.
In any of the embodiments described herein, the transducer treatment depth can be approximately 0.5 mm, 1 mm, 1.5 mm, 2 mm, 3 mm, 4 mm, 4.5 mm, 5 mm, 6 mm, 10 mm 15 mm, 20 mm, 25 mm, or any other depth in the range of 0-100 mm. Varied depth treatment, including treatment of the same tissue at different depths or treatment of different tissues, can increase clinical results by providing synergistic effects.
In various embodiments of the present invention, a transducer 280 is capable of emitting ultrasound energy for imaging, diagnostics, or treating and combinations thereof. In one embodiment, the transducer 280 is configured to emit ultrasound energy at a specific depth in a region of interest to target a region of interest of a specific tissue such as a corrugator supercilii muscle as described below. In this embodiment, the transducer 280 may be capable of emitting unfocused or defocused ultrasound energy over a wide area of the region of interest 65 for treatment purposes (see
In one embodiment, an emitter-receiver module 200 is configured with a treatment frequency of approximately 4 MHz, a treatment depth of approximately 4.5 mm and an imaging depth range of roughly 0-8 mm. In one embodiment, an emitter-receiver module 200 is configured with a treatment frequency of approximately 7 MHz, a treatment depth of approximately 3.0 mm and an imaging depth range of roughly 0-8 mm. In one embodiment, an emitter-receiver module 200 is configured with a treatment frequency of approximately 7 MHz, a treatment depth of approximately 4.5 mm and an imaging depth range of roughly 0-8 mm.
Transducer 280 may comprise one or more transducers for facilitating imaging and/or treatment. The transducer 280 may comprise a piezoelectrically active material, such as, for example, lead zirconante titanate, or other piezoelectrically active materials such as, but not limited to, a piezoelectric ceramic, crystal, plastic, and/or composite materials, as well as lithium niobate, lead titanate, barium titanate, and/or lead metaniobate, including piezoelectric, electrically conductive, and plastic film layers deposited on spherically focused backing material. In addition to, or instead of, a piezoelectrically active material, the transducer 280 may comprise any other materials configured for generating radiation and/or acoustical energy. The transducer 280 may also comprise one or more matching and/or backing layers coupled to the piezoelectrically active material. The transducer 280 may also be configured with single or multiple damping elements.
In one embodiment, the thickness of a transduction element of the transducer 280 may be configured to be uniform. That is, the transduction element may be configured to have a thickness that is generally substantially the same throughout. In another embodiment, the transduction element may also be configured with a variable thickness, and/or as a multiple damped device. For example, the transduction element of the transducer 280 may be configured to have a first thickness selected to provide a center operating frequency of a lower range, for example from about 1 MHz to about 10 MHz. The transduction element may also be configured with a second thickness selected to provide a center operating frequency of a higher range, for example from about 10 MHz to greater than 100 MHz.
In yet another embodiment, the transducer 280 is configured as a single broadband transducer excited with two or more frequencies to provide an adequate output for raising a temperature within a treatment area of the region of interest to the desired level as discussed herein. The transducer 280 may be configured as two or more individual transducers, such that each transducer 280 may comprise a transduction element. The thickness of the transduction elements may be configured to provide center-operating frequencies in a desired treatment range. For example, in one embodiment, the transducer 280 may comprise a first transducer configured with a first transduction element having a thickness corresponding to a center frequency range of about 1 MHz to about 10 MHz, and a second transducer configured with a second transduction element having a thickness corresponding to a center frequency range of about 10 MHz to greater than 100 MHz. Various other combinations and ranges of thickness for a first and/or second transduction element can be designed to focus at specific depths below a surface 501, for specific frequency ranges, and/or specific energy emissions.
The transduction elements of the transducer 280 can be configured to be concave, convex, and/or planar. In one embodiment, the transduction elements are configured to be concave in order to provide focused energy for treatment of the region of interest. Additional embodiments of transducers are disclosed in U.S. patent application Ser. No. 10/944,500, entitled “System and Method for Variable Depth Ultrasound Treatment,” incorporated in its entirety herein by reference.
Moreover, the transducer 280 can be any distance from the surface 501. In that regard, it can be far away from the surface 501 disposed within a long transducer or it can be just a few millimeters from the surface 501. This distance can be determined by design using the offset distance 270 as described herein. In certain embodiments, positioning the transducer 280 closer to the surface 501 is better for emitting ultrasound at higher frequencies. Moreover, both two and three dimensional arrays of elements can be used in the present invention. Furthermore, the transducer 280 may comprise a reflective surface, tip, or area at the end of the transducer 280 that emits ultrasound energy. This reflective surface may enhance, magnify, or otherwise change ultrasound energy emitted from the CTS 20.
In various embodiments any set of one or more transducers 280 can be used for various functions, such as separate treat/image or dual-mode (both treat/image) transducers or a treat-only version. In various embodiments the imaging element(s) can be on the side (adjacent to) or at any relative position, attitude, and/or height, or even within the therapy element(s). One or more therapy depths and frequencies can be used and one or more imaging elements or one or more dual-mode elements. In various embodiments any controllable means of moving the active transduction element(s) within the emitter-receiver module 200 housing constitute viable embodiments.
In various embodiments, the emitter-receiver module 200 can also be configured in various manners and comprise a number of reusable and/or disposable components and parts in various embodiments to facilitate its operation. For example, the emitter-receiver module 200 can be configured within any type of transducer probe housing or arrangement for facilitating the coupling of the transducer 280 to a tissue interface, with such housing comprising various shapes, contours and configurations. The emitter-receiver module 200 can comprise any type of matching, such as for example, electric matching, which may be electrically switchable, multiplexer circuits and/or aperture/element selection circuits, and/or probe identification devices, to certify probe handle, electric matching, transducer usage history and calibration, such as one or more serial EEPROM (memories).
In various embodiments, the emitter-receiver module 200 may also comprise cables and connectors, motion mechanisms, motion sensors and encoders, thermal monitoring sensors, and/or user control and status related switches, and indicators such as LEDs. In one embodiment, a motion mechanism similar to the motion mechanism 400 described in the hand wand 100 may be used to drive the emitter-receiver module 200 from within the emitter-receiver module 200. In one embodiment, a hand wand 100 is electrically connectable to the emitter-receiver module 200 to drive the emitter-receiver module 200 from within itself. In various embodiments, a motion mechanism (in any of the embodiments described herein) may be used to controllably create multiple lesions, or sensing of probe motion itself may be used to controllably create multiple lesions and/or stop creation of lesions 550, as discussed herein. For example in one embodiment, for safety reasons if the emitter-receiver module 200 is suddenly jerked or is dropped, a sensor can relay this action to the controller 300 to initiate a corrective action or shut down the emitter-receiver module 200. In addition, an external motion encoder arm may be used to hold the probe during use, whereby the spatial position and attitude of the emitter-receiver module 200 is sent to the controller 300 to help controllably create lesions 550. Furthermore, other sensing functionality such as profilometers or other imaging modalities may be integrated into the emitter-receiver module 200 in accordance with various embodiments. In one embodiment, pulse-echo signals to and from the emitter/receiver module 200 are utilized for tissue parameter monitoring of the treatment region 550.
Coupling components can comprise various devices to facilitate coupling of the emitter-receiver module 200 to a region of interest. For example, coupling components can comprise cooling and acoustic coupling system configured for acoustic coupling of ultrasound energy and signals. Acoustic cooling/coupling system with possible connections such as manifolds may be utilized to couple sound into the region-of-interest, control temperature at the interface and deeper into tissue, provide liquid-filled lens focusing, and/or to remove transducer waste heat. The coupling system may facilitate such coupling through use of one or more coupling mediums, including air, gases, water, liquids, fluids, gels, solids, and/or any combination thereof, or any other medium that allows for signals to be transmitted between the transducer 280 and a region of interest. In one embodiment one or more coupling media is provided inside a transducer. In one embodiment a fluid-filled emitter-receiver module 200 contains one or more coupling media inside a housing. In one embodiment a fluid-filled emitter-receiver module 200 contains one or more coupling media inside a sealed housing, which is separable from a dry portion of an ultrasonic device.
In addition to providing a coupling function, in accordance with one embodiment, the coupling system can also be configured for providing temperature control during the treatment application. For example, the coupling system can be configured for controlled cooling of an interface surface or region between the emitter-receiver module 200 and a region of interest and beyond by suitably controlling the temperature of the coupling medium. The suitable temperature for such coupling medium can be achieved in various manners, and utilize various feedback systems, such as thermocouples, thermistors or any other device or system configured for temperature measurement of a coupling medium. Such controlled cooling can be configured to further facilitate spatial and/or thermal energy control of the emitter-receiver module 200.
In one embodiment, the emitter-receiver module 200 is connected to a motion mechanism 400 in the hand wand 100. In one embodiment, the motion mechanism 400 may be in the emitter-receiver module 200. One embodiment of a motion mechanism 400 is illustrated in
A sensor 425 operates as one embodiment of a position sensor by reading an encoder 430 which is mounted on the scotch yoke 403. In one embodiment, the encoder strip 430 is an optical encoder which has a pitch in a range from about 1.0 mm to about 0.01 mm. In one embodiment, the pitch may be about 0.1 mm. The encoder strip 430 can include index marks at each end of its travel. The direction of travel of the encoder strip 430 can be determined by comparing phases of two separate channels in the optical sensor 425. In one embodiment, the encoder strip 430 has one, two or more home positions which may be useful in calibrating for a position and travel of the scotch yoke 403.
In one embodiment, the movement of the scotch yoke 403 is transferred through the movement mechanism 432 such that the transducer 280 moves in a linear fashion inside of the emitter-receiver module 200. In one embodiment, the scotch yoke 403 includes a movement member 432 and a magnetic coupling 433 on a distal end of the movement member 432. The movement member 432 can be sized to travel through or within a liquid-tight seal.
Transducer 280 can have a travel distance 272 The coupling system may facilitate such coupling With reference to
According to various embodiments, when the emitter-receiver module 200 is coupled to the surface 501, which may be a skin surface of the subject, the CTS 20 can image and/or treat a treatment area 272. In some aspects of these embodiments, the imaging by the CTS 20 can be over essentially the entire treatment area 272 at specified depths 278 below the surface 501. In some aspects of these embodiments, the treatment can include discrete energy emissions 50 to create lesion 550 at intervals along the treatment area 272 and at specified depths 278. In one embodiment the intervals are discrete. In one embodiment the intervals are overlapping.
In various embodiments the imaging subsystem 350 may be operated in a B-mode. The imaging subsystem 350 can provide support to the emitter-receiver module 200 such that the emitter-receiver module 200 can have emission energy 50 from a frequency of about 10 MHz to greater than 100 MHz. In one embodiment, the frequency is about 18 MHz. In one embodiment, the frequency is about 25 MHz. The imaging subsystem 350 can support any frame rate that may be useful for the applications. In some embodiments, the frame rate may be in a range from about 1 frames per second (hereinafter “FPS”) to about 100 FPS, or from about 5 FPS to about 50 FPS or from about 5 FPS to about 20 FPS nominal. An image field of view may be controlled by the image area of the transducer 280 in a focus of the transducer 280 at a specific depth 278 below the surface 501 as discussed herein. In various embodiments, the field of view can be less than 20 mm in depth and 100 mm in width or less than 10 mm in depth and less than 50 mm in width. In one embodiment, a particularly useful image field of view is about 8 mm in depth by about 25 mm in width.
A resolution of the field of view can be controlled by the graduation of the movement mechanism 400. As such, any pitch may be useful based on the graduation of the motion mechanism 400. In one embodiment, the resolution of the field of view may be controlled by the resolution of an encoder 430 and sensor 425. In one embodiment the image field of view can have a pitch in the range of 0.01 mm to 0.5 mm or from about 0.05 mm to about 0.2 mm. In one embodiment, a particularly useful line pitch for the image field of view is about 0.1 mm.
According to various embodiments, the imaging subsystem 350 can include one or more functions. In one embodiment, the one or more functions can include any of the following B-mode, scan image, freeze image, image brightness, distance calipers, text annotation for image, save image, print image, and/or combinations thereof. In various embodiments of the present invention, the imaging subsystem 350 contains pulse echo imaging electronics.
Various embodiments of the therapy subsystem 320 comprise a radio frequency (hereinafter “RF”) driver circuit which can deliver and/or monitor power going to the transducer 280. In one embodiment, the therapy subsystem 320 can control an acoustic power of the transducer 280. In one embodiment, the acoustic power can be from a range of 1 watt (hereinafter “W”) to about 100 W in a frequency range from about 1 MHz to about 10 MHz, or from about 10 W to about 50 W at a frequency range from about 3 MHz to about 8 MHz. In one embodiment, the acoustic power and frequencies are about 40 W at about 4.3 MHz and about 30 W at about 7.5 MHz. An acoustic energy produced by this acoustic power can be between about 0.01 joule (hereinafter “J”) to about 10 J or about 2 J to about 5 J. In one embodiment, the acoustic energy is in a range less than about 3 J.
In various embodiments the therapy subsystem 320 can control a time on for the transducer 280. In one embodiment, the time on can be from about 1 millisecond (hereinafter “ms”) to about 100 ms or about 10 ms to about 50 ms. In one embodiment, time on periods can be about 30 ms for a 4.3 MHz emission and about 30 ms for a 7.5 MHz emission.
In various embodiments, the therapy subsystem 320 can control the drive frequency of the transducer 280 moving across the travel 272. In various embodiments, the frequency of the transducer 280 is based on the emitter/receiver 200 connected to the hand wand 100. According to some embodiments, the frequency of this movement may be in a range from about 1 MHz to about 10 MHz, or about 4 MHz to about 8 MHz. In one embodiment, the frequencies of this movement are about 4.3 MHz or about 7.5 MHz. As discussed herein, the length of the travel 272 can be varied, and in one embodiment, the travel 272 has a length of about 25 mm.
According to various embodiments, the therapy subsystem 320 can control the line scan along the travel 272 and this line scan can range from 0 to the length of the distal of the travel 272. In one embodiment, the line scan can be in a range from about 0 to about 25 mm. According to one embodiment, the line scan can have incremental energy emissions 50 having a treatment spacing 295 and this treatment spacing can range from about 0.01 mm to about 25 mm or from 0.2 mm to about 2.0 mm. In one embodiment, treatment spacing 295 is about 1.5 mm. In various embodiments, the treatment spacing 295 can be predetermined, constant, variable, programmable, and/or changed at any point before, during or after a treatment line. The resolution of the line scan is proportional to the resolution of the motion mechanism 400. In various embodiments, the resolution that is controllable by the therapy subsystem 320 is equivalent to the resolution controllable by the imaging subsystem 350 and, as such, can be in the same range as discussed for the imaging subsystem 350.
In various embodiments, the therapy subsystem 320 can have one or more functions. In one embodiment, the one or more functions can include any of the following: emission energy control, treatment spacing, travel length, treatment ready, treatment, treatment stop, save record, print record, display treatment, and/or combinations thereof.
In various embodiments, the control subsystem 340 includes electronic hardware which mechanically scans the transducer 280 for one or more functions. In one embodiment, one or more functions that can be scanned by the controller subsystem 340 can include scanning the transducer 280 for imaging, a position of the transducer 280 for imaging, scan slip positions of the transducer 280 at locations for therapy, controls therapy hardware settings, provides other control functions, interfacing with the embedded host 330, and/or combinations thereof. In one embodiment the locations are discrete. In one embodiment the locations are overlapping.
In various embodiments, an embedded host 330 is in two-way communication with the controller 340 and the graphical interface 310. In one embodiment, data from the controller 340 can be converted to a graphical format by the embedded host 330 and then transferred to the graphical interface 310 for displaying imaging and/or treatment data.
In one embodiment, commands can be entered by a user employing the graphical interface 310. The commands entered by use of the graphical interface 310 can be communicated to embedded host 330 and then communicated to controller 340 for control and operation of the therapy subsystem 320, the imaging subsystem 350, the hand wand 100, and/or the emitter-receiver module 200. In various embodiments, the embedded host 330 can include a processing unit, memory, and/or software.
In various embodiments, when the imaging button 150 is pressed the CTS 20 enters an imaging sequence in which the imaging subsystem 350 acquires scan lines which are transferred to the embedded host 330 for data conversion and/or graphical conversion which is then communicated to the graphical interface 310. While the system is operating in the imaging sequence, the imaging button 150 may be pressed again which puts the CTS 20 into a ready state. In an aspect of this embodiment, an audio warning or visual display such as the indicator 155 may be initiated to alert the user that the CTS 20 is in the ready state. In the ready state, the controller subsystem 340 communicates with the embedded host 330 to acquire users entered treatment settings. These treatment settings can be checked and can be verified and converted to hardware parameter in the controller subsystem 340. In one embodiment, such set hardware parameters can include treatment timing, cadence, time on, time off, RF driver power, voltage levels, acoustic power output, oscillator frequency, therapy transducer frequency, treatment spacing, travel, motion mechanism speed, and/or combinations thereof. The CTS 20 may remain in the ready state indefinitely or may be timed out after a set time period.
In various embodiments of the present invention, when the CTS 20 is in the ready state, the treatment button 160 may be activated. This activation of the treatment button 160 commences a treatment sequence. The treatment sequence is controllable by the therapy subsystem 320 which executes the treatment sequence along with the controller subsystem 340 and independently of the embedded host 330. The treatment sequence is delivered in real time and last one of the length of the activating of the treatment button 160 or a programmed time downloaded from the embedded host 330 into the controller subsystem 340 and/or the therapy subsystem 320.
In various embodiments, safety features can be designed in the CTS 20 to ensure safe use, imaging, and treatment. In various embodiments, the embedded host 330 is in communication with data port 390 which can comprise either one-way or two-way communication between the data port 390 and the embedded host 330. The data port 390 can interface any electronic storage device, for example, the data port 390 can be interfaced for one or more of a USB drive, a compact flash drive, a secured digital card, a compact disc, and the like. In one embodiment, a storage device through data port 390 to the embedded host 330 can download treatment records or software updates. In another aspect of these embodiments, the storage device can be a two-way communication through data port 390 to the embedded host 330 such that a treatment protocol can be downloaded to the embedded host 330 and CTS 20. A treatment protocol can include parameters, imaging data, treatment data, date/time, treatment duration, subject information, treatment location, and combinations thereof, and the like which can be uploaded by and/or downloaded from the embedded host 330 to the storage device via the data port 390. In one embodiment, a second data port (not shown) may be located on the back of the controller. The second data port may provide power and/or data to a printer.
In various embodiments, the CTS 20 includes a lock 395. In one embodiment, in order to operate CTS 20, lock 395 must be unlocked so that power switch 393 may be activated. In one embodiment, the power may remain on as the lock 395 is unlocked and locked successively and different parameters are entered. A key 396 (not illustrated) may be needed to unlock the lock 395. Examples of keys 396 useful herein include a standard metal tooth and groove key, or an electronic key. In some embodiments, an electronic key 396 may be digitally encoded to include user information and collect data and/or time usage of CTS 20. In one embodiment, an electronic key is particularly useful with CTS 20 may be a USB drive with encryption such that inserting the USB drive key into lock 395 the CTS 20 may be activated. In various embodiments, a software key can be configured to indicate a condition or status to the user, lock the system, interrupt the system, or other feature.
With reference to
The graphical interface 310 displays images and systems status as well as facilitates the user interface for entering commands to control the CTS 20. The controller subsystem 340 can control the imaging subsystem 350, the therapy subsystem 320, as well as interfacing and communicating treatment protocol to the hand wand 100 and the emitter-receiver module 200, as described herein. In one embodiment, the controller subsystem 340 not only sets treatment parameters but also monitors the status of such treatment and transfers such status to the host 330 for display on display/touch screen 310. The front panel flex circuit 345 can be a printed circuit cable that connects the controller 300 to the interface cable 130. In one embodiment, the cable 130 can include a quick connect or release, multi-pin connector plug which interfaces to the front panel flex circuit 345 as described herein. The cable 130 allows for interfacing of the controller 300 with the hand wand 100 and the emitter-receiver module 200 as described herein.
Now with reference to
In various embodiments of the present invention, the emitter-receiver module 200 can include a probe ID and connector PCB 224. The probe ID and connector PCB can include a secure EEPROM. The probe ID and connector PCB 224 can be interfaced with a PCB located in a dry portion of the emitter-receiver module 200 and interfaced with the transducer 280 The transducer 280 is typically located in the liquid portion of the emitter-receiver module 200. In one embodiment, the emitter-receiver module 200 can be connected to the hand wand 100 via the spring pin flex 106 and spring pin connector 422 which can be a twelve contact spring pin connector that is recessed in the hand wand 100. The spring pin flex 106 with its twelve contact spring pin connector can be connected to the probe ID and connector PCB 224 which can include gold plated contacts. In one embodiment, the probe ID and connector PCB 224 can include a usage counter that disables the emitter-receiver module 200 after a pre-set usage. In various embodiments, the pre-set usage can range from a single treatment sequence to multiple treatment sequences. In one embodiment, the pre-set usage is determined by a pre-set time on of the transducer 280. In one embodiment, the pre-set usage is a single cycle of treatment sequences. In this aspect, essentially the emitter-receiver module 200 is disposable after each use. In one embodiment, the system automatically shuts off or otherwise indicates to a user that the emitter-receiver module 200 should be replaced. The system may be programmed to shut off or otherwise indicate replacement based on at least one of usage time, energy delivered, shelf time, or a combination thereof.
With further reference to
The imaging sub-circuits 110 can include a time gain control amplifier and tunable bypass filter which can receive echoes produced by the imaging portion of the transducer 280. The imaging can be controlled by imaging switch 150. Power can be transferred from the controller 300 via cable 130. Such power can be directed to the imaging sub-circuits 110, the image switch 150 and the treatment switch 160. Such power can also be provided to the stepper motor 402, the encoder 425, the probe IO switch 181, the hand wand temperature sensor 183, and a hand wand ID EEPROM 169. All of the electronics described in
The emitter-receiver module 200 includes an interface connectable to the hand wand 100 as described in
Since it is possible for a user to potentially touch the spring pin flex contacts 422 when an emitter-receiver module 200 is not attached, the current must be able to be turned off in this situation to provide safety to the user. To provide such safety, contact pins 422 on opposite ends of the spring pin flex 106 can be used to detect an attachment of the emitter-receiver module 200 to the hand wand 100. As discussed above, motion mechanism 400 can be connected to the transducer 280 to provide linear movement of the transducer along the travel 272.
In various embodiments, the CTS 20 can include various safety features to provide a safe environment for the user and/or the subject that receives treatment. One embodiment, the CTS 20 can include at least one of calibration data, safe operating area, high mismatch detect, high current detect, RF driver supply voltage monitoring, forward and reverse electric power monitoring, acoustic coupling detection, acoustic coupling complete, treatment position sensing, and combinations thereof.
For example, calibration data can include certain characteristics for a given emitter-receiver module 200 that reside on the storage device 249. Such characteristics can include but are not limited to unique and traceable serial numbers, probe identification, frequency setting, acoustic power versus voltage lookup table, electric power versus voltage lookup table, maximum power levels, date codes, usage, other information, and/or combinations thereof. For example, a safe operating area safety feature limits energy output for a given emitter-receiver module 200 is limited to a safe operating area. Such a limitation may include for a given emitter-receiver module 200, the acoustic power level supplied by the power supply voltage and the time On may be limited in the hardware and/or software of the controller 300 and/or the emitter-receiver module 200.
An example of a high mismatch detect safety feature can include if a fault occurs in reflective power from the load of the emitter-receiver module 200 is large as compared a forward power such as the emitter-receiver module 200 failure, open circuit, or high reflective energy, then a system Stop state would automatically and indefinitely be invoked by comparator circuit latched in the hardware of the controller 300 and a notification of such fault would appear on the display/touch screen 310 to alert the user. An example of a high current detect safety feature can include if a driver fault or load fault occurs such that a large current draw is detected such as for example a short circuit or electrical component failure, then a Stop state would be automatically and immediately invoked as located in the hardware of the controller 300 and a notice would be displayed on the display/touch screen 310 to alert the user.
An example of RF driver supply voltage monitoring safety feature can include the CTS 20 measuring the RF driver power supply voltage setting before, during and after treatment to assure that the voltage is at the correct level. If it is determined that the voltage is outside the correct level, then a Stop state would be automatically and immediately invoked and a notice would be displayed on the display/touch screen 310 to alert the user. An example of a safety feature includes monitoring the stepper motor 402 during treatment and determining if it is in an acceptable range such that the transducer 280 is properly moving along the travel 272 at a predetermined rate or frequency. If it is determined that the stepper motor 402 is not at an expected position, a notification is issued to alert the user.
An example of an acoustic coupling safety feature includes an imaging sequence that indicates to the user that the emitter-receiver module 200 is acoustically coupled to the surface 501 before and after treatment. An image sequence confirms that the transducer 280 is scanning a treatment area.
Still further, other safety features may be included such as thermal monitoring, use of a stop switch, a probe sensor, or a combination thereof. An example of thermal monitoring can include monitoring the temperature of the liquid portion of the emitter-receiver module 200, monitoring the temperature of the hand wand 100, monitoring the temperature of the controller 300, monitoring the temperature of the controller subsystem 340 and/or monitoring the temperature of the RF driver 352. Such temperature monitoring assures that the devices described operate within temperatures that are acceptable and will provide notification if a temperature is outside an acceptable range thus alerting the user.
A stop switch can be included in CTS 20 such that when a user hits the stop switch the system moves to a safe and inactive state upon activation of the stop switch. An example of a probe sense fail safe can include immediately stopping imaging and/or treatment if the emitter-receiver module 200 is disconnected from the hand wand 100 while in use. In one embodiment, the CTS 20 can include a system diagnostic which can include software checks for errors, unexpected events and usage. The system diagnostics may also include maintenance indicator that tracks the usage of the CTS 20 and notifies the user that maintenance is needed for the system. Other safety features may be included in the CTS 20 that are well known in the art such as fuses, system power supply over voltage and over current limiting, as well as standardized protections such as fire safety ratings, electrical safety ratings, ISO\EN 60601 compliance and the like.
In various embodiments, the CTS 20 includes a removable transducer module 200 interfaced to a hand enclosure 100 having at least one controller button (150 and/or 160) such that the transducer module 200 and the controller button (150 and/or 160) is operable using only one hand. In an aspect of the embodiments, the transducer module 200 provides ultrasound energy for an imaging function and/or a treatment function. In another aspect of the embodiments, the device includes a controller 300 coupled to the hand-held enclosure 100 and interfaced to the transducer module 200. In a further aspect of these embodiments, the controller 300 controls the ultrasound energy of and receives a signal from the transducer module 200. The controller 300 can have a power supply providing power for the ultrasound energy. In still another aspect of the embodiments, the device is used in aesthetic imaging and treatment on a brow of a patient.
Facial muscle tissue is capable of contraction and expansion. Skeletal muscle is a fibrous tissue used to generate stress and strain. For example, skeletal muscles in the forehead region can produce frowning and wrinkles. There are several facial muscles within the brow or forehead including the epicranius muscle, the corrugator supercilii muscle, and the procerus muscle. These facial muscles are responsible for movement of the forehead and various facial expressions. Besides facial muscles, other tissues exist in the brow region that also can lead to wrinkles on the brow.
In accordance with one embodiment of the present invention, methods for ultrasound cosmetic treatment of tissue using one cosmetic treatment system are provided. The ultrasound energy can be focused, unfocused or defocused and is applied to a ROI 65 containing one of facial muscle tissue or dermal layers or fascia to achieve a therapeutic effect, such as a tighten of a brow of a subject 500.
In various embodiments, certain cosmetic procedures that are traditionally performed through invasive techniques are accomplished by targeting energy such as ultrasound energy at specific subcutaneous tissues 510. In one embodiment, methods for non-invasively treating subcutaneous tissues 510 to perform a brow life are provided. In one embodiment, a non-invasive brow lift is performed by applying ultrasound energy at specific depths 278 along the brow to ablatively cut, cause tissue to be reabsorbed into the body, coagulate, remove, manipulate, or paralyze subcutaneous tissue 510 such as the facial muscle 509, for example, the corrugator supercilii muscle, the epicranius muscle, and the procerus muscle within the brow to reduce wrinkles.
In some embodiments, ultrasound energy is applied at a ROI 65 along a patient's forehead. The ultrasound energy can be applied at specific depths and is capable of targeting certain subcutaneous tissues within the brow such as with reference to
For example, the corrugator supercilii muscle in a target zone 525, can be targeted and treated by the application of ultrasound energy at specific depths 278. This facial muscle 509 or other subcutaneous facial muscles can be ablated, coagulated, micro-ablated, shaped or otherwise manipulated by the application of ultrasound energy in a non-invasive manner. Specifically, instead of cutting a corrugator supercilii muscle during a classic or endoscopic brow lift, the targeted muscle 509 such as the corrugator supercilii can be ablated, micro-ablated, or coagulated by applying ultrasound energy at the forehead without the need for traditional invasive techniques.
One method is configured for targeted treatment of subcutaneous tissue 510 in the forehead region 65 in various manners such as through the use of therapy only, therapy and monitoring, imaging and therapy, or therapy, imaging and monitoring. Targeted therapy of tissue can be provided through ultrasound energy delivered at desired depths 278 and locations via various spatial and temporal energy settings. In one embodiment, the tissues of interest are viewed in motion in real time by utilizing ultrasound imaging to clearly view the moving tissue to aid in targeting and treatment of a ROI 65 on the patient's forehead. Therefore, the practitioner or user performing the non-invasive brow lift can visually observe the movement and changes occurring to the subcutaneous tissue 510 during treatment.
In one embodiment, CTS 20 generates ultrasound energy which is directed to and focused below the surface 501. This controlled and focused ultrasound energy creates the lesion 550 which may be a thermally coagulated zone or void in subcutaneous tissue 510. In one embodiment, the emitted energy 50 raises a temperature of the tissue at a specified depth 278 below the surface 501. The temperature of the tissue can be raised from about 1° C. to about 100° C. above an ambient temperature of the tissue, or about 5° C. to about 60° C. above an ambient temperature of the tissue or above 10° C. to about 50° C. above the ambient temperature of the tissue. In some embodiments, the emitted energy 50 targets the tissue below the surface 501 which cuts, ablates, coagulates, micro-ablates, manipulates, and/or causes a lesion 550 in the tissue portion 10 below the surface 501 at a specified depth 278. In one embodiment, during the treatment sequence, the transducer 280 moves in a direction denoted by the arrow marked 290 at specified intervals 295 to create a series of treatment zones 254 each of which receives an emitted energy 50 to create a lesion 550. For example, the emitted energy 50 creates a series of lesions 550 in the facial muscle layer 509 of tissue portion 10.
In various embodiments, delivery of emitted energy 50 at a suitable depth 278, distribution, timing, and energy level is provided by the emitter-receiver module 200 through controlled operation by the control system 300 to achieve the desired therapeutic effect of controlled thermal injury to treat at least one of the dermis layer 503, fat layer 505, the SMAS layer 507 and the facial muscle layer 509. During operation, the emitter-receiver module 200 and/or the transducer 280 can also be mechanically and/or electronically scanned along the surface 501 to treat an extended area. In addition, spatial control of a treatment depth 278 can be suitably adjusted in various ranges, such as between a wide range of about 0 mm to about 25 mm, suitably fixed to a few discrete depths, with an adjustment limited to a fine range, for example, approximately between about 3 mm to about 9 mm, and/or dynamically adjusted during treatment, to treat at least one of the dermis layer 503, fat layer 505, the SMAS layer 507 and the facial muscle layer 509. Before, during, and after the delivery of ultrasound energy 50 to at least one of the dermis layer 503, fat layer 505, the SMAS layer 507 and the facial muscle layer 509, monitoring of the treatment area and surrounding structures can be provided to plan and assess the results and/or provide feedback to the controller 300 and the user via the graphical interface 310.
As to the treatment of the SMAS layer 507 and similar fascia, connective tissue can be permanently tightened by thermal treatment to temperatures about 60° C. or higher. Upon ablating, collagen fibers shrink immediately by approximately 30% of their length. The shrunken fibers can produce tightening of the tissue, wherein the shrinkage should occur along the dominant direction of the collagen fibers. Throughout the body, collagen fibers are laid down in connective tissues along the lines of chronic stress (tension). On the aged face, the collagen fibers of the SMAS 507 region are predominantly oriented along the lines of gravitational tension. Shrinkage of these fibers results in tightening of the SMAS 507 in the direction desired for correction of laxity and sagging due to aging. The treatment includes the ablation of specific regions of the SMAS 507 region and similar suspensory connective tissues.
In addition, the SMAS layer 507 varies in depth and thickness at different locations, for example from about 0.5 mm to about 5 mm or more. On the face, important structures such as nerves, parotid gland, arteries and veins are present over, under or near the SMAS 507 region. Treating through localized heating of regions of the SMAS 507 layer or other suspensory subcutaneous tissue 510 to temperatures of about 60° C. to about 90° C., without significant damage to overlying or distal/underlying tissue, or proximal tissue, as well as the precise delivery of therapeutic energy to the SMAS layer 507, and obtaining feedback from the region of interest before, during, and after treatment can be suitably accomplished through the CTS 20.
In various embodiments, a method is provided for performing a brow lift on a patient. In some embodiments, the method includes coupling a probe 200 to a brow region 65 of the patient 60 and imaging at least a portion of subcutaneous tissue 510 of the brow region to determine a target area in the subcutaneous tissue 510. In an aspect of the embodiment, the method includes administering ultrasound energy 50 into the target area 525 in the subcutaneous tissue 510 to ablate the subcutaneous tissue 510 in the target area 525, which causes tightening of a dermal layer 503 above the subcutaneous tissue 510 of the brow region 65.
In various embodiments, a method is provided for tightening a portion of a dermal layer 503 on a facial area of a patient 60. In some embodiments, the method includes inserting a transducer module 200 into a hand controller 100 and then coupling the transducer module 200 to a facial area of the patient 60. In one embodiment, the method includes activating a first switch 150 on the hand controller 100 to initiate an imaging sequence of a portion of tissue 10 below the dermal layer 503, then collecting data from the imaging sequence. In this embodiment, the method includes calculating a treatment sequence from the collected data, and activating a second switch 160 on the hand controller 100 to initiate the treatment sequence. In an aspect of the embodiments, the method can be useful on a portion of a face, head, neck and/or other part of the body of a patient 60.
With reference to
Turning to
Step 803 moves to step 804 which is the administering of energy to the target zone 525. For example, step 804 can be illustrated in, for example,
With reference to
The system function tabs 1000 reflect aspects of the system function. In one embodiment, the interactive graphical display 310 has one or more general functions. In various embodiments the interactive graphical display 310 has two, three, four or more general functions. In one embodiment, an interactive graphical display 310 has three general functions: a planning function, a imaging/treatment function, and a settings function. In one embodiment, the planning function contains the controls and information instrumental in planning a treatment, which can automatically set therapy controls. In one embodiment, the planning function can display an overview of the various treatment regions with recommended treatment parameters for each. For example, parameters for treating such regions as the forehead, left or right temple, left or right preauricular, left or right neck, submental, and left or right cheek can show a recommended emitter-receiver module 200 listing energy levels and recommended numbers of lines of treatment. Certain areas can include a protocol listing for selection of treatment protocols, a protocol allowed treat regions listing, and disallowed regions that can not be selected due to an incorrect transducer, which can be grayed out. In one embodiment, the imaging/treatment function contains the controls and protocol information needed for imaging soft tissue and for treating pertinent soft tissue. In various embodiments, a start up screen can include patient and/or facility data. In one embodiment the imaging/treatment function can include a main startup screen. In one embodiment a imaging/treatment function can be configured for a forehead. The settings function allows the user to input, track, store and/or print patient treatment information outside the scanning function, and can include such information as patient and facility information, end treatment, treatment records, images, help, volume, and system shutdown controls and dialogs.
The therapy controls 1010 can set acoustic energy level, spacing for setting the distance between micro-coagulative zones, and length which can set the maximum distance of the treatment line and similar information.
The imaging controls 1020 can include marker (not scanning), display (scanning), image and scan information. The marker can include a distance icon to show calipers and text for annotation. The display can increase or decrease brightness or other display related characteristics. The image icon can toggle a treat ruler, or save an image. The scan buttons can start or stop scanning for imaging purposes and similar information.
The region control 1030 launches a dialog below the image to select tissue region. The patient total line count 1040 keeps track of the cumulative number of treatment lines delivered and similar information. The treat zone line count 1050 indicates a zone of treatment, such as forehead or submental, etc. and can display the lines delivered to a zone or a protocol for recommended lines and similar information. The system status 1060 can display that the system is ready, treating, or other mode-dependent system messages and similar information. The probe information area 1070 can display the name of the attached transducer, the treatment depth of the transducer, and the number of lines spent/(vs.) total line capacity of transducer and similar information. The header information 1080 can include the facility, clinician, patient name and patient identification, date and time and similar information. The image-treat region 1090 can include an ultrasound image, horizontal and vertical (depth) rulers with 1 mm tick marks or other measuring dimensions, a treatment ruler indicating spacing, length and depth of treatment, and other similar information.
One benefit or advantage of using a treatment system that also allows imaging is that a user can verify that there sufficient coupling between the transducer and the skin (such as by applying coupling gel between the emitter-receiver module 200 and skin) by ensuring there are not dark, vertical bars, as indicative of air pockets between the face of the transducer and patient. A lack of coupling may result in a region that is improperly treated. Corrective action might include placing more coupling ultrasound gel to ensure proper contact and communication between the device and the patient.
Therapeutic treatment can be initiated by pressing the treatment button 160 on the hand wand 100. In one embodiment, an indicator 155 will display a yellow light to indicate the system is in the “treating” state. As the energy 50 is delivered a continuous tone is sounded and a yellow ‘treating’ line will advance over the green ‘ready’ treatment line on the screen. To deliver the next line of energy in the same treatment area, the user can advance the transducer roughly 1-6 mm, or roughly 2-3 mm (depending on the treatment, region, etc.) to adjacent tissue and press the treatment button 160 again. In various embodiments, a time period can elapse between delivering a previous line of energy 50. In various embodiments, the time period can be 1 second, 5 seconds, 10 seconds, or any other duration. In one embodiment, if five or ten seconds (or some other duration) have elapsed between delivering the previous line of energy 50, the user can press the imaging button 150 on the hand wand 100 to restore the “ready” state, and then press the treatment button 160 next to it. Treatment can continue in this fashion until the recommended number of lines (as shown on the bottom/center of the screen) has been delivered. In one embodiment, when the correct number of lines is delivered, the line count color turns from orange to white.
In one embodiment, the settings function allows a user to export images. Stored images are listed in the bottom dialog box and the most recently user-selected image is displayed above it. If an external storage device and/or printer is attached then image file export and/or printing is enabled, respectively. In one embodiment, the settings function allows a user to export records.
In certain embodiments, the interactive graphical display 310 can display error messages to direct appropriate user responses, such as in one embodiment of an error message.
The citation of references herein does not constitute admission that those references are prior art or have relevance to the patentability of the teachings disclosed herein. All references cited in the Description section of the specification are hereby incorporated by reference in their entirety for all purposes. In the event that one or more of the incorporated references, literature, and similar materials differs from or contradicts this application, including, but not limited to, defined terms, term usage, described techniques, or the like, this application controls.
Some embodiments and the examples described herein are examples and not intended to be limiting in describing the full scope of compositions and methods of these invention. Equivalent changes, modifications and variations of some embodiments, materials, compositions and methods can be made within the scope of the present invention, with substantially similar results.
This application is a continuation of U.S. patent application Ser. No. 17/410,780, filed Aug. 24, 2021 and issued as U.S. Pat. No. 10,537,304, which is a continuation of U.S. patent application Ser. No. 16/703,019, filed Dec. 4, 2019 and issued as U.S. Pat. No. 11,123,039, which is a continuation of U.S. patent application Ser. No. 12/996,616, filed Jan. 12, 2011 and issued as U.S. Pat. No. 10,537,304, which is a U.S. National Phase under 35 U.S.C. 371 of International Application No. PCT/US2009/046475, filed Jun. 5, 2009 and published in English on Dec. 10, 2009, which claims the benefit of priority from U.S. Provisional No. 61/059,477 filed Jun. 6, 2008, each of which is incorporated in its entirety by reference, herein. Any and all priority claims identified in the Application Data Sheet, or any correction thereto, are hereby incorporated by reference under 37 CFR 1.57.
Number | Name | Date | Kind |
---|---|---|---|
2427348 | Bond et al. | Sep 1947 | A |
2792829 | Calosi | Feb 1952 | A |
3913386 | Saglio | Oct 1975 | A |
3965455 | Hurwitz | Jun 1976 | A |
3992925 | Perilhou | Nov 1976 | A |
4039312 | Patru | Aug 1977 | A |
4059098 | Murdock | Nov 1977 | A |
4101795 | Fukumoto | Jul 1978 | A |
4151834 | Sato et al. | May 1979 | A |
4166967 | Benes et al. | Sep 1979 | A |
4211948 | Smith et al. | Jul 1980 | A |
4211949 | Brisken et al. | Jul 1980 | A |
4213344 | Rose | Jul 1980 | A |
4276491 | Daniel | Jun 1981 | A |
4315514 | Drewes et al. | Feb 1982 | A |
4325381 | Glenn | Apr 1982 | A |
4343301 | Indech | Aug 1982 | A |
4372296 | Fahim | Feb 1983 | A |
4379145 | Masuho et al. | Apr 1983 | A |
4381007 | Doss | Apr 1983 | A |
4381787 | Hottinger | May 1983 | A |
4397314 | Vaguine | Aug 1983 | A |
4409839 | Taenzer | Oct 1983 | A |
4417170 | Benisncasa | Nov 1983 | A |
4431008 | Wanner et al. | Feb 1984 | A |
4441486 | Pounds | Apr 1984 | A |
4452084 | Taenzer | Jun 1984 | A |
4484569 | Driller | Nov 1984 | A |
4507582 | Glenn | Mar 1985 | A |
4513749 | Kino | Apr 1985 | A |
4513750 | Heyman et al. | Apr 1985 | A |
4527550 | Ruggera et al. | Jul 1985 | A |
4528979 | Marchenko | Jul 1985 | A |
4534221 | Fife et al. | Aug 1985 | A |
4566459 | Umemura et al. | Jan 1986 | A |
4567895 | Putzke | Feb 1986 | A |
4586512 | Do-Huu | May 1986 | A |
4587971 | Stolfi | May 1986 | A |
4601296 | Yerushalmi | Jul 1986 | A |
4620546 | Aida et al. | Nov 1986 | A |
4637256 | Sugiyama et al. | Jan 1987 | A |
4646756 | Watmough | Mar 1987 | A |
4663358 | Hyon | May 1987 | A |
4668516 | Duraffourd et al. | May 1987 | A |
4672591 | Breimesser et al. | Jun 1987 | A |
4680499 | Umemura et al. | Jul 1987 | A |
4697588 | Reichenberger | Oct 1987 | A |
4754760 | Fukukita et al. | Jul 1988 | A |
4757820 | Itoh | Jul 1988 | A |
4771205 | Mequio | Sep 1988 | A |
4801459 | Liburdy | Jan 1989 | A |
4803625 | Fu et al. | Feb 1989 | A |
4807633 | Fry | Feb 1989 | A |
4817615 | Fukukita et al. | Apr 1989 | A |
4858613 | Fry | Aug 1989 | A |
4860732 | Hasegawa et al. | Aug 1989 | A |
4865041 | Hassler | Sep 1989 | A |
4865042 | Umemura | Sep 1989 | A |
4867169 | Machida | Sep 1989 | A |
4874562 | Hyon | Oct 1989 | A |
4875487 | Seppi | Oct 1989 | A |
4881212 | Takeuchi | Nov 1989 | A |
4891043 | Zeimer et al. | Jan 1990 | A |
4893624 | Lele | Jan 1990 | A |
4896673 | Rose | Jan 1990 | A |
4900540 | Ryan et al. | Feb 1990 | A |
4901729 | Saitoh | Feb 1990 | A |
4917096 | Englehart | Apr 1990 | A |
4932414 | Coleman et al. | Jun 1990 | A |
4938216 | Lele | Jul 1990 | A |
4938217 | Lele | Jul 1990 | A |
4947046 | Kawabata et al. | Aug 1990 | A |
4951653 | Fry | Aug 1990 | A |
4955365 | Fry | Sep 1990 | A |
4958626 | Nambu | Sep 1990 | A |
4976709 | Sand | Dec 1990 | A |
4979501 | Valchanov | Dec 1990 | A |
4992989 | Watanabe et al. | Feb 1991 | A |
5012797 | Liang | May 1991 | A |
5018508 | Fry et al. | May 1991 | A |
5030874 | Saito et al. | Jul 1991 | A |
5036855 | Fry | Aug 1991 | A |
5040537 | Katakura | Aug 1991 | A |
5054310 | Flynn | Oct 1991 | A |
5054470 | Fry | Oct 1991 | A |
5054491 | Saito et al. | Oct 1991 | A |
5070879 | Herres | Dec 1991 | A |
5088495 | Miyagawa | Feb 1992 | A |
5115814 | Griffith | May 1992 | A |
5117832 | Sanghvi | Jun 1992 | A |
5123418 | Saurel | Jun 1992 | A |
5142511 | Kanai et al. | Aug 1992 | A |
5143063 | Fellner | Sep 1992 | A |
5143074 | Dory | Sep 1992 | A |
5149319 | Unger | Sep 1992 | A |
5150711 | Dory | Sep 1992 | A |
5150714 | Green | Sep 1992 | A |
5152294 | Mochizuki et al. | Oct 1992 | A |
5156144 | Iwasaki | Oct 1992 | A |
5158536 | Sekins | Oct 1992 | A |
5159931 | Pini | Nov 1992 | A |
5163421 | Bernstein | Nov 1992 | A |
5163436 | Saitoh et al. | Nov 1992 | A |
5178135 | Uchiyama et al. | Jan 1993 | A |
5190518 | Takasu | Mar 1993 | A |
5190766 | Ishihara | Mar 1993 | A |
5191880 | McLeod | Mar 1993 | A |
5205287 | Erbel et al. | Apr 1993 | A |
5209720 | Unger | May 1993 | A |
5212671 | Fujii et al. | May 1993 | A |
5215680 | D'Arrigo | Jun 1993 | A |
5224467 | Oku | Jul 1993 | A |
5230334 | Klopotek | Jul 1993 | A |
5230338 | Allen et al. | Jul 1993 | A |
5247924 | Suzuki et al. | Sep 1993 | A |
5255681 | Ishimura et al. | Oct 1993 | A |
5257970 | Dougherty | Nov 1993 | A |
5265614 | Hayakawa | Nov 1993 | A |
5267985 | Shimada | Dec 1993 | A |
5269297 | Weng | Dec 1993 | A |
5282797 | Chess | Feb 1994 | A |
5295484 | Marcus | Mar 1994 | A |
5295486 | Wollschlager et al. | Mar 1994 | A |
5304169 | Sand | Apr 1994 | A |
5305756 | Entrekin et al. | Apr 1994 | A |
5321520 | Inga et al. | Jun 1994 | A |
5323779 | Hardy et al. | Jun 1994 | A |
5327895 | Hashimoto et al. | Jul 1994 | A |
5329202 | Garlick et al. | Jul 1994 | A |
5348016 | Unger et al. | Sep 1994 | A |
5358466 | Aida et al. | Oct 1994 | A |
5360268 | Hayashi | Nov 1994 | A |
5370121 | Reichenberger | Dec 1994 | A |
5370122 | Kunig | Dec 1994 | A |
5371483 | Bhardwaj | Dec 1994 | A |
5375602 | Lancee et al. | Dec 1994 | A |
5379773 | Hornsby | Jan 1995 | A |
5380280 | Peterson | Jan 1995 | A |
5380519 | Schneider et al. | Jan 1995 | A |
5383917 | Desai et al. | Jan 1995 | A |
5391140 | Schaetzle et al. | Feb 1995 | A |
5391197 | Burdette et al. | Feb 1995 | A |
5392259 | Bolorforosh | Feb 1995 | A |
5396143 | Seyed-Bolorforosh et al. | Mar 1995 | A |
5398689 | Connor et al. | Mar 1995 | A |
5406503 | Williams | Apr 1995 | A |
5413550 | Castel | May 1995 | A |
5417216 | Tanaka | May 1995 | A |
5423220 | Finsterwald et al. | Jun 1995 | A |
5435311 | Umemura | Jul 1995 | A |
5438998 | Hanafy | Aug 1995 | A |
5443068 | Cline et al. | Aug 1995 | A |
5445611 | Eppstein et al. | Aug 1995 | A |
5458596 | Lax | Oct 1995 | A |
5460179 | Okunuki et al. | Oct 1995 | A |
5460595 | Hall et al. | Oct 1995 | A |
5419327 | Rohwedder | Nov 1995 | A |
5469854 | Unger et al. | Nov 1995 | A |
5471488 | Fujio | Dec 1995 | A |
5472405 | Buchholtz et al. | Dec 1995 | A |
5487388 | Rello et al. | Jan 1996 | A |
5492126 | Hennige | Feb 1996 | A |
5496256 | Bock | Mar 1996 | A |
5501655 | Rolt | Mar 1996 | A |
5503152 | Oakley et al. | Apr 1996 | A |
5503320 | Webster et al. | Apr 1996 | A |
5507790 | Weiss | Apr 1996 | A |
5511296 | Dias et al. | Apr 1996 | A |
5520188 | Hennige | May 1996 | A |
5522869 | Burdette | Jun 1996 | A |
5523058 | Umemura et al. | Jun 1996 | A |
5524620 | Rosenchein | Jun 1996 | A |
5524624 | Tepper | Jun 1996 | A |
5524625 | Okazaki | Jun 1996 | A |
5526624 | Berg | Jun 1996 | A |
5526812 | Dumoulin et al. | Jun 1996 | A |
5526814 | Cline et al. | Jun 1996 | A |
5526815 | Granz | Jun 1996 | A |
5529070 | Augustine et al. | Jun 1996 | A |
5540235 | Wilson | Jul 1996 | A |
5558092 | Unger | Sep 1996 | A |
5560362 | Sliwa et al. | Oct 1996 | A |
5573497 | Chapelon | Nov 1996 | A |
5575291 | Hayakawa | Nov 1996 | A |
5575807 | Faller | Nov 1996 | A |
5577502 | Darrow et al. | Nov 1996 | A |
5577507 | Snyder et al. | Nov 1996 | A |
5577991 | Akui et al. | Nov 1996 | A |
5580575 | Unger et al. | Dec 1996 | A |
5643179 | Fujimoto | Jan 1997 | A |
5601526 | Chapelon | Feb 1997 | A |
5603323 | Pflugrath et al. | Feb 1997 | A |
5605154 | Ries et al. | Feb 1997 | A |
5609562 | Kaali | Mar 1997 | A |
5615091 | Palatnik | Mar 1997 | A |
5618275 | Bock | Apr 1997 | A |
5620479 | Diederich | Apr 1997 | A |
5622175 | Sudol et al. | Apr 1997 | A |
5617858 | Taverna et al. | May 1997 | A |
5638819 | Manwaring et al. | Jun 1997 | A |
5644085 | Lorraine et al. | Jul 1997 | A |
5647373 | Paltieli | Jul 1997 | A |
5655535 | Frlemel et al. | Aug 1997 | A |
5655538 | Lorraine | Aug 1997 | A |
5657760 | Ying | Aug 1997 | A |
5658328 | Johnson | Aug 1997 | A |
5660836 | Knowlton | Aug 1997 | A |
5662116 | Kondo | Sep 1997 | A |
5665053 | Jacobs | Sep 1997 | A |
5665141 | Vago | Sep 1997 | A |
5671746 | Dreschel et al. | Sep 1997 | A |
5673699 | Trahey et al. | Oct 1997 | A |
5676692 | Sanghvi | Oct 1997 | A |
5685820 | Riek et al. | Nov 1997 | A |
5690608 | Watanabe | Nov 1997 | A |
5694936 | Fujimoto | Dec 1997 | A |
5697897 | Buchholtz | Dec 1997 | A |
5701900 | Shehada et al. | Dec 1997 | A |
5704361 | Seward et al. | Jan 1998 | A |
5706252 | Le Verrier et al. | Jan 1998 | A |
5706564 | Rhyne | Jan 1998 | A |
5715823 | Wood et al. | Feb 1998 | A |
5720287 | Chapelon et al. | Feb 1998 | A |
5722411 | Suzuki | Mar 1998 | A |
5727554 | Kalend et al. | Mar 1998 | A |
5735280 | Sherman et al. | Apr 1998 | A |
5740804 | Cerofolini | Apr 1998 | A |
5743863 | Chapelon | Apr 1998 | A |
5746005 | Steinberg | May 1998 | A |
5746762 | Bass | May 1998 | A |
5748767 | Raab | May 1998 | A |
5749364 | Sliwa et al. | May 1998 | A |
5755228 | Wilson et al. | May 1998 | A |
5755753 | Knowlton | May 1998 | A |
5762066 | Law | Jun 1998 | A |
5763886 | Schulte | Jun 1998 | A |
5769790 | Watkins | Jun 1998 | A |
5779644 | Eberle et al. | Jul 1998 | A |
5792058 | Lee | Aug 1998 | A |
5795297 | Daigle | Aug 1998 | A |
5795311 | Wess | Aug 1998 | A |
5810009 | Mine et al. | Sep 1998 | A |
5810888 | Fenn | Sep 1998 | A |
5814599 | Mitragotri et al. | Sep 1998 | A |
5817013 | Ginn et al. | Oct 1998 | A |
5817021 | Reichenberger | Oct 1998 | A |
5820564 | Slayton | Oct 1998 | A |
5823962 | Schaetzle | Oct 1998 | A |
5827204 | Grandia et al. | Oct 1998 | A |
5840032 | Hatfield et al. | Nov 1998 | A |
5844140 | Seale | Dec 1998 | A |
5853367 | Chalek et al. | Dec 1998 | A |
5866024 | de Villeneuve | Feb 1999 | A |
5869751 | Bonin | Feb 1999 | A |
5871524 | Knowlton | Feb 1999 | A |
5873902 | Sanghvi | Feb 1999 | A |
5876341 | Wang et al. | Mar 1999 | A |
5879303 | Averkiou et al. | Mar 1999 | A |
5882557 | Hayakawa | Mar 1999 | A |
5884627 | Wakabayashi et al. | Mar 1999 | A |
5891034 | Bucholz | Apr 1999 | A |
5895356 | Andrus et al. | Apr 1999 | A |
5899861 | Friemel et al. | May 1999 | A |
5904659 | Duarte | May 1999 | A |
5919219 | Knowlton | Jul 1999 | A |
5923099 | Bili | Jul 1999 | A |
5924989 | Polz | Jul 1999 | A |
5928169 | Schatzle et al. | Jul 1999 | A |
5931805 | Brisken | Aug 1999 | A |
5938606 | Bonnefous | Aug 1999 | A |
5938612 | Kline-Schoder | Aug 1999 | A |
5948011 | Knowlton | Sep 1999 | A |
5957844 | Dekel | Sep 1999 | A |
5957882 | Nita et al. | Sep 1999 | A |
5957941 | Ream | Sep 1999 | A |
5964707 | Fenster et al. | Oct 1999 | A |
5967980 | Ferre et al. | Oct 1999 | A |
5968034 | Fullmer | Oct 1999 | A |
5971949 | Levin | Oct 1999 | A |
5977538 | Unger et al. | Nov 1999 | A |
5984881 | Ishibashi et al. | Nov 1999 | A |
5984882 | Rosenchein | Nov 1999 | A |
5990598 | Sudol et al. | Nov 1999 | A |
5997471 | Gumb et al. | Dec 1999 | A |
5997497 | Nita et al. | Dec 1999 | A |
5999843 | Anbar | Dec 1999 | A |
6004262 | Putz et al. | Dec 1999 | A |
6007499 | Martin et al. | Dec 1999 | A |
6013032 | Savord | Jan 2000 | A |
6014473 | Hossack et al. | Jan 2000 | A |
6016255 | Bolan et al. | Jan 2000 | A |
6019724 | Gronningsaeter et al. | Feb 2000 | A |
6022308 | Williams | Feb 2000 | A |
6022317 | Cruanas et al. | Feb 2000 | A |
6022327 | Chang | Feb 2000 | A |
6030374 | McDaniel | Feb 2000 | A |
6036646 | Barthe | Mar 2000 | A |
6039048 | Silberg | Mar 2000 | A |
6039689 | Lizzi | Mar 2000 | A |
6042556 | Beach | Mar 2000 | A |
6049159 | Barthe | Apr 2000 | A |
6050943 | Slayton | Apr 2000 | A |
6059727 | Fowlkes | May 2000 | A |
6071239 | Cribbs | Jun 2000 | A |
6080108 | Dunham | Jun 2000 | A |
6083148 | Williams | Jul 2000 | A |
6086535 | Ishibashi | Jul 2000 | A |
6086580 | Mordon et al. | Jul 2000 | A |
6090054 | Tagishi | Jul 2000 | A |
6093148 | Fujimoto | Jul 2000 | A |
6093883 | Sanghvi | Jul 2000 | A |
6100626 | Frey et al. | Aug 2000 | A |
6101407 | Groezinger | Aug 2000 | A |
6106469 | Suzuki et al. | Aug 2000 | A |
6113558 | Rosenchein | Sep 2000 | A |
6113559 | Klopotek | Sep 2000 | A |
6120452 | Barthe | Sep 2000 | A |
6123081 | Durette | Sep 2000 | A |
6126619 | Peterson et al. | Oct 2000 | A |
6135971 | Hutchinson | Oct 2000 | A |
6139499 | Wilk | Oct 2000 | A |
6159150 | Yale et al. | Dec 2000 | A |
6171244 | Finger et al. | Jan 2001 | B1 |
6176840 | Nishimura | Jan 2001 | B1 |
6183426 | Akisada | Feb 2001 | B1 |
6183502 | Takeuchi | Feb 2001 | B1 |
6183773 | Anderson | Feb 2001 | B1 |
6190323 | Dias | Feb 2001 | B1 |
6190336 | Duarte | Feb 2001 | B1 |
6193658 | Wendelken | Feb 2001 | B1 |
6198956 | Dunne | Mar 2001 | B1 |
6210327 | Brackett et al. | Apr 2001 | B1 |
6213948 | Barthe | Apr 2001 | B1 |
6216029 | Paltieli | Apr 2001 | B1 |
6233476 | Strommer et al. | May 2001 | B1 |
6234990 | Rowe et al. | May 2001 | B1 |
6241753 | Knowlton | Jun 2001 | B1 |
6246898 | Vesely et al. | Jun 2001 | B1 |
6251074 | Averkiou et al. | Jun 2001 | B1 |
6251088 | Kaufman et al. | Jun 2001 | B1 |
6268405 | Yao | Jul 2001 | B1 |
6273864 | Duarte | Aug 2001 | B1 |
6280402 | Ishibashi et al. | Aug 2001 | B1 |
6287257 | Matichuk | Sep 2001 | B1 |
6287304 | Eggers et al. | Sep 2001 | B1 |
6296619 | Brisken | Oct 2001 | B1 |
6301989 | Brown et al. | Oct 2001 | B1 |
6307302 | Toda | Oct 2001 | B1 |
6309355 | Cain et al. | Oct 2001 | B1 |
6311090 | Knowlton | Oct 2001 | B1 |
6315741 | Martin | Nov 2001 | B1 |
6322509 | Pan et al. | Nov 2001 | B1 |
6322532 | D'Sa | Nov 2001 | B1 |
6325540 | Lounsberry et al. | Dec 2001 | B1 |
6325758 | Carol et al. | Dec 2001 | B1 |
6325769 | Klopotek | Dec 2001 | B1 |
6325798 | Edwards et al. | Dec 2001 | B1 |
6350276 | Knowlton | Feb 2002 | B1 |
6356780 | Licato et al. | Mar 2002 | B1 |
6361531 | Hissong | Mar 2002 | B1 |
6370411 | Osadchy et al. | Apr 2002 | B1 |
6375672 | Aksan | Apr 2002 | B1 |
6377854 | Knowlton | Apr 2002 | B1 |
6377855 | Knowlton | Apr 2002 | B1 |
6381497 | Knowlton | Apr 2002 | B1 |
6381498 | Knowlton | Apr 2002 | B1 |
6387380 | Knowlton | May 2002 | B1 |
6390982 | Bova et al. | May 2002 | B1 |
6405090 | Knowlton | Jun 2002 | B1 |
6409720 | Hissong | Jun 2002 | B1 |
6413216 | Cain et al. | Jul 2002 | B1 |
6413253 | Koop | Jul 2002 | B1 |
6413254 | Hissong | Jul 2002 | B1 |
6419648 | Vitek | Jul 2002 | B1 |
6423007 | Lizzi et al. | Jul 2002 | B2 |
6425865 | Salcudean | Jul 2002 | B1 |
6425867 | Vaezy | Jul 2002 | B1 |
6425912 | Knowlton | Jul 2002 | B1 |
6428477 | Mason | Aug 2002 | B1 |
6428532 | Doukas | Aug 2002 | B1 |
6430446 | Knowlton | Aug 2002 | B1 |
6432057 | Mazess et al. | Aug 2002 | B1 |
6432067 | Martin | Aug 2002 | B1 |
6432101 | Weber | Aug 2002 | B1 |
6436061 | Costantino | Aug 2002 | B1 |
6438424 | Knowlton | Aug 2002 | B1 |
6440071 | Slayton | Aug 2002 | B1 |
6440121 | Weber | Aug 2002 | B1 |
6443914 | Costantino | Sep 2002 | B1 |
6447443 | Keogh et al. | Sep 2002 | B1 |
6450979 | Miwa et al. | Sep 2002 | B1 |
6451013 | Bays et al. | Sep 2002 | B1 |
6453202 | Knowlton | Sep 2002 | B1 |
6461304 | Tanaka et al. | Oct 2002 | B1 |
6461378 | Knowlton | Oct 2002 | B1 |
6470216 | Knowlton | Oct 2002 | B1 |
6338716 | Hossack | Nov 2002 | B1 |
6485420 | Bullis | Nov 2002 | B1 |
6488626 | Lizzi | Dec 2002 | B1 |
6491657 | Rowe | Dec 2002 | B2 |
6500121 | Slayton | Dec 2002 | B1 |
6500141 | Irion | Dec 2002 | B1 |
6506171 | Vitek et al. | Jan 2003 | B1 |
6508774 | Acker | Jan 2003 | B1 |
6511427 | Sliwa, Jr. et al. | Jan 2003 | B1 |
6511428 | Azuma | Jan 2003 | B1 |
6514244 | Pope | Feb 2003 | B2 |
6517484 | Wilk | Feb 2003 | B1 |
6524250 | Weber | Feb 2003 | B1 |
6666835 | Martin | Mar 2003 | B2 |
6540679 | Slayton | Apr 2003 | B2 |
6540685 | Rhoads et al. | Apr 2003 | B1 |
6540700 | Fujimoto et al. | Apr 2003 | B1 |
6547788 | Maguire et al. | Apr 2003 | B1 |
6554771 | Buil et al. | Apr 2003 | B1 |
6569099 | Babaev | May 2003 | B1 |
6569108 | Sarvazyan et al. | May 2003 | B2 |
6572552 | Fukukita | Jun 2003 | B2 |
6575956 | Brisken et al. | Jun 2003 | B1 |
6595934 | Hissong | Jul 2003 | B1 |
6599256 | Acker | Jul 2003 | B1 |
6605043 | Dreschel | Aug 2003 | B1 |
6605080 | Altshuler et al. | Aug 2003 | B1 |
6607498 | Eshel | Aug 2003 | B2 |
6618620 | Freundlich et al. | Sep 2003 | B1 |
6623430 | Slayton | Sep 2003 | B1 |
6626854 | Friedman | Sep 2003 | B2 |
6626855 | Weng | Sep 2003 | B1 |
6638226 | He et al. | Oct 2003 | B2 |
6645145 | Dreschel et al. | Nov 2003 | B1 |
6645150 | Angelsen et al. | Nov 2003 | B2 |
6645162 | Friedman | Nov 2003 | B2 |
6662054 | Kreindel | Dec 2003 | B2 |
6663627 | Francischelli | Dec 2003 | B2 |
6665806 | Shimizu | Dec 2003 | B1 |
6669638 | Miller | Dec 2003 | B1 |
6673017 | Jackson | Jan 2004 | B1 |
6685639 | Wang et al. | Feb 2004 | B1 |
6685640 | Fry | Feb 2004 | B1 |
6692450 | Coleman | Feb 2004 | B1 |
6699237 | Weber | Mar 2004 | B2 |
6716184 | Vaezy et al. | Apr 2004 | B2 |
6719449 | Laughlin | Apr 2004 | B1 |
6719694 | Weng | Apr 2004 | B2 |
6726627 | Lizzi et al. | Apr 2004 | B1 |
6733449 | Krishnamurthy et al. | May 2004 | B1 |
6749624 | Knowlton | Jun 2004 | B2 |
6772490 | Toda | Aug 2004 | B2 |
6773409 | Truckai et al. | Aug 2004 | B2 |
6775404 | Pagoulatos et al. | Aug 2004 | B1 |
6790187 | Thompson et al. | Sep 2004 | B2 |
6824516 | Batten et al. | Nov 2004 | B2 |
6825176 | White et al. | Nov 2004 | B2 |
6835940 | Morikawa et al. | Dec 2004 | B2 |
6846290 | Lizzi et al. | Jan 2005 | B2 |
6875176 | Mourad et al. | Apr 2005 | B2 |
6882884 | Mosk et al. | Apr 2005 | B1 |
6887239 | Elstrom | May 2005 | B2 |
6887260 | McDaniel | May 2005 | B1 |
6889089 | Behl | May 2005 | B2 |
6896657 | Willis | May 2005 | B2 |
6902536 | Manna | Jun 2005 | B2 |
6905466 | Salgo | Jun 2005 | B2 |
6918907 | Kelly | Jul 2005 | B2 |
6920883 | Bessette | Jul 2005 | B2 |
6921371 | Wilson | Jul 2005 | B2 |
6932771 | Whitmore | Aug 2005 | B2 |
6932814 | Wood | Aug 2005 | B2 |
6936044 | McDaniel | Aug 2005 | B2 |
6936046 | Hissong | Aug 2005 | B2 |
6945937 | Culp et al. | Sep 2005 | B2 |
6948843 | Laugharn et al. | Sep 2005 | B2 |
6953941 | Nakano et al. | Oct 2005 | B2 |
6958043 | Hissong | Oct 2005 | B2 |
6971994 | Young et al. | Dec 2005 | B1 |
6974417 | Lockwood | Dec 2005 | B2 |
6976492 | Ingle | Dec 2005 | B2 |
6992305 | Maezawa et al. | Jan 2006 | B2 |
6997923 | Anderson | Feb 2006 | B2 |
7006874 | Knowlton | Feb 2006 | B2 |
7020528 | Neev | Mar 2006 | B2 |
7022089 | Ooba | Apr 2006 | B2 |
7058440 | Heuscher et al. | Jun 2006 | B2 |
7063666 | Weng | Jun 2006 | B2 |
7070565 | Vaezy et al. | Jul 2006 | B2 |
7074218 | Washington et al. | Jul 2006 | B2 |
7094252 | Koop | Aug 2006 | B2 |
7108663 | Talish et al. | Sep 2006 | B2 |
7115123 | Knowlton | Oct 2006 | B2 |
7122029 | Koop et al. | Oct 2006 | B2 |
7142905 | Slayton | Nov 2006 | B2 |
7165451 | Brooks et al. | Jan 2007 | B1 |
7179238 | Hissong | Feb 2007 | B2 |
7189230 | Knowlton | Mar 2007 | B2 |
7229411 | Slayton | Jun 2007 | B2 |
7235592 | Muratoglu | Jun 2007 | B2 |
7258674 | Cribbs | Aug 2007 | B2 |
7273459 | Desilets | Sep 2007 | B2 |
7294125 | Phalen et al. | Nov 2007 | B2 |
7297117 | Trucco | Nov 2007 | B2 |
7303555 | Makin et al. | Dec 2007 | B2 |
7311679 | Desilets et al. | Dec 2007 | B2 |
7327071 | Nishiyama et al. | Feb 2008 | B2 |
7331951 | Eshel et al. | Feb 2008 | B2 |
7332985 | Larson et al. | Feb 2008 | B2 |
7338434 | Haarstad et al. | Mar 2008 | B1 |
7347855 | Eshel | Mar 2008 | B2 |
RE40403 | Cho et al. | Jun 2008 | E |
7393325 | Barthe | Jul 2008 | B2 |
7398116 | Edwards | Jul 2008 | B2 |
7399279 | Abend et al. | Jul 2008 | B2 |
7491171 | Barthe et al. | Feb 2009 | B2 |
7507235 | Keogh et al. | Mar 2009 | B2 |
7510536 | Foley et al. | Mar 2009 | B2 |
7517315 | Willis | Apr 2009 | B2 |
7530356 | Slayton | May 2009 | B2 |
7530958 | Slayton | May 2009 | B2 |
7532201 | Quistgaard et al. | May 2009 | B2 |
7571336 | Barthe | Aug 2009 | B2 |
7601120 | Moilanen et al. | Oct 2009 | B2 |
7615015 | Coleman | Nov 2009 | B2 |
7615016 | Barthe | Nov 2009 | B2 |
7652411 | Crunkilton et al. | Jan 2010 | B2 |
7662114 | Seip et al. | Feb 2010 | B2 |
7674257 | Pless et al. | Mar 2010 | B2 |
7686763 | Vaezy et al. | Mar 2010 | B2 |
7713203 | Lacoste et al. | Mar 2010 | B2 |
7694406 | Wildes et al. | Apr 2010 | B2 |
7695437 | Quistgaard et al. | Apr 2010 | B2 |
7727156 | Angelsen et al. | Jun 2010 | B2 |
7758524 | Barthe | Jul 2010 | B2 |
7766848 | Desilets et al. | Aug 2010 | B2 |
7789841 | Huckle et al. | Sep 2010 | B2 |
7806839 | Mast et al. | Oct 2010 | B2 |
7815570 | Eshel et al. | Oct 2010 | B2 |
7819826 | Diederich et al. | Oct 2010 | B2 |
7828734 | Azhari et al. | Oct 2010 | B2 |
7824348 | Barthe | Nov 2010 | B2 |
7833162 | Hasegawa et al. | Nov 2010 | B2 |
7841984 | Cribbs et al. | Nov 2010 | B2 |
7846096 | Mast et al. | Dec 2010 | B2 |
7857773 | Desilets et al. | Dec 2010 | B2 |
7875023 | Eshel et al. | Jan 2011 | B2 |
7901359 | Mandrusov et al. | Mar 2011 | B2 |
7905007 | Calisti et al. | Mar 2011 | B2 |
7905844 | Desilets et al. | Mar 2011 | B2 |
7914453 | Slayton et al. | Mar 2011 | B2 |
7914469 | Torbati | Mar 2011 | B2 |
7955281 | Pedersen et al. | Jun 2011 | B2 |
7967764 | Lidgren et al. | Jun 2011 | B2 |
7967839 | Flock et al. | Jun 2011 | B2 |
7955262 | Rosenberg | Jul 2011 | B2 |
7993289 | Quistgaard et al. | Aug 2011 | B2 |
8057465 | Sliwa, Jr. et al. | Sep 2011 | B2 |
8057389 | Barthe et al. | Nov 2011 | B2 |
8066641 | Barthe et al. | Nov 2011 | B2 |
8123707 | Huckle et al. | Feb 2012 | B2 |
8128618 | Gliklich et al. | Mar 2012 | B2 |
8133180 | Slayton et al. | Mar 2012 | B2 |
8133191 | Rosenberg et al. | Mar 2012 | B2 |
8142200 | Crunkilton et al. | Mar 2012 | B2 |
8152904 | Slobodzian et al. | Apr 2012 | B2 |
8162858 | Manna et al. | Apr 2012 | B2 |
8166332 | Barthe et al. | Apr 2012 | B2 |
8182428 | Angelsen et al. | May 2012 | B2 |
8197409 | Foley et al. | Jun 2012 | B2 |
8206299 | Foley et al. | Jun 2012 | B2 |
8208346 | Crunkilton | Jun 2012 | B2 |
8211017 | Foley et al. | Jul 2012 | B2 |
8262591 | Pedersen et al. | Sep 2012 | B2 |
8262650 | Zanelli et al. | Sep 2012 | B2 |
8264126 | Toda et al. | Sep 2012 | B2 |
8273037 | Kreindel et al. | Sep 2012 | B2 |
8282554 | Makin et al. | Oct 2012 | B2 |
8292835 | Cimino | Oct 2012 | B1 |
8298163 | Cimino | Oct 2012 | B1 |
8333700 | Barthe et al. | Dec 2012 | B1 |
8334637 | Crunkilton et al. | Dec 2012 | B2 |
8337407 | Quistgaard et al. | Dec 2012 | B2 |
8343051 | Desilets et al. | Jan 2013 | B2 |
8454540 | Eshel et al. | Jan 2013 | B2 |
8366622 | Slayton et al. | Feb 2013 | B2 |
8398549 | Palmeri et al. | Mar 2013 | B2 |
8409097 | Slayton et al. | Apr 2013 | B2 |
8425435 | Wing et al. | Apr 2013 | B2 |
8388535 | Weng et al. | May 2013 | B2 |
8444562 | Barthe et al. | May 2013 | B2 |
8460193 | Barthe et al. | Jun 2013 | B2 |
8480585 | Slayton et al. | Jul 2013 | B2 |
8486001 | Weyant | Jul 2013 | B2 |
8506486 | Slayton et al. | Aug 2013 | B2 |
8512250 | Quistgaard et al. | Aug 2013 | B2 |
8523775 | Barthe et al. | Sep 2013 | B2 |
8523849 | Liu et al. | Sep 2013 | B2 |
8535228 | Slayton et al. | Sep 2013 | B2 |
8570837 | Toda et al. | Oct 2013 | B2 |
8573392 | Bennett et al. | Nov 2013 | B2 |
8583211 | Salomir et al. | Nov 2013 | B2 |
8585618 | Hunziker et al. | Nov 2013 | B2 |
8604672 | Toda et al. | Dec 2013 | B2 |
8622937 | Weng et al. | Jan 2014 | B2 |
8636665 | Slayton et al. | Jan 2014 | B2 |
8641622 | Barthe et al. | Feb 2014 | B2 |
8663112 | Slayton et al. | Mar 2014 | B2 |
8672848 | Slayton et al. | Mar 2014 | B2 |
8690778 | Slayton et al. | Apr 2014 | B2 |
8690779 | Slayton et al. | Apr 2014 | B2 |
8690780 | Slayton et al. | Apr 2014 | B2 |
8708935 | Barthe et al. | Apr 2014 | B2 |
8715186 | Slayton et al. | May 2014 | B2 |
8726781 | Eckhoff et al. | May 2014 | B2 |
8728071 | Lischinsky et al. | May 2014 | B2 |
8753295 | Thierman | Jun 2014 | B2 |
8758253 | Sano et al. | Jun 2014 | B2 |
8836203 | Nobles et al. | Sep 2014 | B2 |
8857438 | Barthe et al. | Oct 2014 | B2 |
8858471 | Barthe et al. | Oct 2014 | B2 |
8915853 | Barthe et al. | Dec 2014 | B2 |
8915854 | Slayton et al. | Dec 2014 | B2 |
8915870 | Barthe et al. | Dec 2014 | B2 |
8920320 | Stecco et al. | Dec 2014 | B2 |
8920324 | Slayton et al. | Dec 2014 | B2 |
8926533 | Bockenstedt et al. | Jan 2015 | B2 |
8932224 | Barthe et al. | Jan 2015 | B2 |
8932238 | Wing et al. | Jan 2015 | B2 |
8968205 | Zeng et al. | Mar 2015 | B2 |
9011336 | Slayton et al. | Apr 2015 | B2 |
9039617 | Slayton et al. | May 2015 | B2 |
9039619 | Barthe et al. | May 2015 | B2 |
9050116 | Homer | Jun 2015 | B2 |
9095697 | Barthe et al. | Aug 2015 | B2 |
9107798 | Azhari et al. | Aug 2015 | B2 |
9114247 | Barthe et al. | Aug 2015 | B2 |
9180314 | Desilets et al. | Nov 2015 | B2 |
9216276 | Slayton et al. | Dec 2015 | B2 |
9220915 | Liu et al. | Dec 2015 | B2 |
9272162 | Slayton et al. | Mar 2016 | B2 |
9283409 | Slayton et al. | Mar 2016 | B2 |
9283410 | Slayton et al. | Mar 2016 | B2 |
9295607 | Rosenberg | Mar 2016 | B2 |
9308390 | Youngquist | Apr 2016 | B2 |
9308391 | Liu et al. | Apr 2016 | B2 |
9314650 | Rosenberg et al. | Apr 2016 | B2 |
9320537 | Slayton et al. | Apr 2016 | B2 |
9345910 | Slayton et al. | May 2016 | B2 |
9421029 | Barthe et al. | Aug 2016 | B2 |
9427600 | Barthe et al. | Aug 2016 | B2 |
9427601 | Barthe et al. | Aug 2016 | B2 |
9433803 | Lin et al. | Sep 2016 | B2 |
9440093 | Homer | Sep 2016 | B2 |
9440096 | Barthe et al. | Sep 2016 | B2 |
9492645 | Zhou et al. | Nov 2016 | B2 |
9492686 | Da Silva | Nov 2016 | B2 |
9498651 | Sapozhnikov et al. | Nov 2016 | B2 |
9510802 | Barthe et al. | Dec 2016 | B2 |
9522290 | Slayton et al. | Dec 2016 | B2 |
9532832 | Ron Edoute et al. | Jan 2017 | B2 |
9533174 | Barthe et al. | Jan 2017 | B2 |
9533175 | Slayton et al. | Jan 2017 | B2 |
9545529 | Britva et al. | Jan 2017 | B2 |
9566454 | Barthe et al. | Feb 2017 | B2 |
9623267 | Ulric et al. | Apr 2017 | B2 |
9694211 | Barthe et al. | Jul 2017 | B2 |
9694212 | Barthe et al. | Jul 2017 | B2 |
9700340 | Barthe et al. | Jul 2017 | B2 |
9707412 | Slayton et al. | Jul 2017 | B2 |
9710607 | Ramdas et al. | Jul 2017 | B2 |
9713731 | Slayton et al. | Jul 2017 | B2 |
9802063 | Barthe et al. | Oct 2017 | B2 |
9827449 | Barthe et al. | Nov 2017 | B2 |
9827450 | Slayton et al. | Nov 2017 | B2 |
9833639 | Slayton et al. | Dec 2017 | B2 |
9833640 | Barthe et al. | Dec 2017 | B2 |
9895560 | Barthe et al. | Feb 2018 | B2 |
9907535 | Barthe et al. | Mar 2018 | B2 |
9919167 | Domankevitz | Mar 2018 | B2 |
9974982 | Slayton et al. | May 2018 | B2 |
9993664 | Aviad et al. | Jun 2018 | B2 |
10010721 | Slayton et al. | Jul 2018 | B2 |
10010724 | Barthe et al. | Jul 2018 | B2 |
10010725 | Slayton et al. | Jul 2018 | B2 |
10010726 | Barthe et al. | Jul 2018 | B2 |
10016626 | Zovrin et al. | Jul 2018 | B2 |
10046181 | Barthe et al. | Aug 2018 | B2 |
10046182 | Barthe et al. | Aug 2018 | B2 |
10070883 | Barthe et al. | Sep 2018 | B2 |
10183183 | Burdette | Jan 2019 | B2 |
10226645 | Barthe | Mar 2019 | B2 |
10238894 | Slayton et al. | Mar 2019 | B2 |
10245450 | Slayton et al. | Apr 2019 | B2 |
10252086 | Barthe et al. | Apr 2019 | B2 |
10265550 | Barthe et al. | Apr 2019 | B2 |
10272272 | Lee et al. | Apr 2019 | B2 |
10300308 | Seip et al. | May 2019 | B2 |
10328289 | Barthe et al. | Jun 2019 | B2 |
10363440 | Cho et al. | Jun 2019 | B2 |
10406383 | Luebcke | Sep 2019 | B2 |
10420960 | Emery | Sep 2019 | B2 |
10420961 | Lacoste | Sep 2019 | B2 |
10485573 | Clark, III et al. | Nov 2019 | B2 |
10492862 | Domankevitz | Dec 2019 | B2 |
10525288 | Slayton et al. | Jan 2020 | B2 |
10532230 | Barthe et al. | Jan 2020 | B2 |
10537304 | Barthe et al. | Jan 2020 | B2 |
10556123 | Altshuler et al. | Feb 2020 | B2 |
10583287 | Schwarz | Mar 2020 | B2 |
10603519 | Slayton et al. | Mar 2020 | B2 |
10603521 | Emery et al. | Mar 2020 | B2 |
10603523 | Slayton et al. | Mar 2020 | B2 |
10610705 | Barthe et al. | Apr 2020 | B2 |
10610706 | Barthe et al. | Apr 2020 | B2 |
10639006 | Choi et al. | May 2020 | B2 |
10639504 | Kim | May 2020 | B2 |
10751246 | Kaila | Aug 2020 | B2 |
10772646 | Lu et al. | Sep 2020 | B2 |
10780298 | Cain et al. | Sep 2020 | B2 |
10888716 | Slayton et al. | Jan 2021 | B2 |
10888717 | Slayton et al. | Jan 2021 | B2 |
10888718 | Barthe et al. | Jan 2021 | B2 |
10960235 | Barthe et al. | Mar 2021 | B2 |
10960236 | Slayton et al. | Mar 2021 | B2 |
11123039 | Barthe et al. | Sep 2021 | B2 |
11167155 | Barthe et al. | Nov 2021 | B2 |
11179580 | Slayton et al. | Nov 2021 | B2 |
11207547 | Slayton et al. | Dec 2021 | B2 |
11207548 | Barthe et al. | Dec 2021 | B2 |
11224895 | Brown et al. | Jan 2022 | B2 |
11235179 | Barthe et al. | Feb 2022 | B2 |
11235180 | Slayton et al. | Feb 2022 | B2 |
11241218 | Emery et al. | Feb 2022 | B2 |
20010009997 | Pope | Jul 2001 | A1 |
20010009999 | Kaufman et al. | Jul 2001 | A1 |
20010014780 | Martin | Aug 2001 | A1 |
20010014819 | Ingle | Aug 2001 | A1 |
20010031922 | Weng | Oct 2001 | A1 |
20010039380 | Larson et al. | Nov 2001 | A1 |
20010041880 | Brisken | Nov 2001 | A1 |
20020000763 | Jones | Jan 2002 | A1 |
20020002345 | Marlinghaus | Jan 2002 | A1 |
20020040199 | Klopotek | Apr 2002 | A1 |
20020040442 | Ishidera | Apr 2002 | A1 |
20020055702 | Atala | May 2002 | A1 |
20020062077 | Emmenegger | May 2002 | A1 |
20020062142 | Knowlton | May 2002 | A1 |
20020072691 | Thompson et al. | Jun 2002 | A1 |
20020082528 | Friedman | Jun 2002 | A1 |
20020082529 | Suorsa et al. | Jun 2002 | A1 |
20020082589 | Friedman | Jun 2002 | A1 |
20020087080 | Slayton | Jul 2002 | A1 |
20020095143 | Key | Jul 2002 | A1 |
20020099094 | Anderson | Jul 2002 | A1 |
20020111569 | Rosenschien et al. | Aug 2002 | A1 |
20020115917 | Honda et al. | Aug 2002 | A1 |
20020128639 | Pless et al. | Aug 2002 | A1 |
20020128648 | Weber | Sep 2002 | A1 |
20020143252 | Dunne et al. | Oct 2002 | A1 |
20020156400 | Babaev | Oct 2002 | A1 |
20020161357 | Anderson | Oct 2002 | A1 |
20020165529 | Danek | Nov 2002 | A1 |
20020168049 | Schriever | Nov 2002 | A1 |
20020169394 | Eppstein et al. | Nov 2002 | A1 |
20020169442 | Neev | Nov 2002 | A1 |
20020173721 | Grunwald et al. | Nov 2002 | A1 |
20020193784 | McHale et al. | Dec 2002 | A1 |
20020193831 | Smith | Dec 2002 | A1 |
20030009153 | Brisken et al. | Jan 2003 | A1 |
20030014039 | Barzell et al. | Jan 2003 | A1 |
20030018255 | Martin | Jan 2003 | A1 |
20030018270 | Makin et al. | Jan 2003 | A1 |
20030023283 | McDaniel | Jan 2003 | A1 |
20030028111 | Vaezy et al. | Feb 2003 | A1 |
20030028113 | Gilbert et al. | Feb 2003 | A1 |
20030032900 | Ella | Feb 2003 | A1 |
20030036706 | Slayton et al. | Feb 2003 | A1 |
20030040739 | Koop | Feb 2003 | A1 |
20030050678 | Sierra | Mar 2003 | A1 |
20030055308 | Friemel et al. | Mar 2003 | A1 |
20030055417 | Truckai et al. | Mar 2003 | A1 |
20030060736 | Martin et al. | Mar 2003 | A1 |
20030065313 | Koop | Apr 2003 | A1 |
20030066708 | Allison et al. | Apr 2003 | A1 |
20030073907 | Taylor | Apr 2003 | A1 |
20030074023 | Kaplan | Apr 2003 | A1 |
20030083536 | Eshel | May 2003 | A1 |
20030092988 | Makin | May 2003 | A1 |
20030097071 | Halmann et al. | May 2003 | A1 |
20030099383 | Lefebvre | May 2003 | A1 |
20030125629 | Ustuner | Jul 2003 | A1 |
20030135135 | Miwa et al. | Jul 2003 | A1 |
20030139790 | Ingle et al. | Jul 2003 | A1 |
20030149366 | Stringer et al. | Aug 2003 | A1 |
20030153961 | Babaev | Aug 2003 | A1 |
20030171678 | Batten et al. | Sep 2003 | A1 |
20030171701 | Babaev | Sep 2003 | A1 |
20030176790 | Slayton | Sep 2003 | A1 |
20030191396 | Sanghvi | Oct 2003 | A1 |
20030199794 | Sakurai et al. | Oct 2003 | A1 |
20030200481 | Stanley | Oct 2003 | A1 |
20030212129 | Liu et al. | Nov 2003 | A1 |
20030212351 | Hissong | Nov 2003 | A1 |
20030212393 | Knowlton | Nov 2003 | A1 |
20030216648 | Lizzi et al. | Nov 2003 | A1 |
20030216795 | Harth | Nov 2003 | A1 |
20030220536 | Hissong | Nov 2003 | A1 |
20030220585 | Hissong | Nov 2003 | A1 |
20030229331 | Brisken et al. | Dec 2003 | A1 |
20030233085 | Giammarusti | Dec 2003 | A1 |
20030236487 | Knowlton | Dec 2003 | A1 |
20040000316 | Knowlton | Jan 2004 | A1 |
20040001809 | Brisken | Jan 2004 | A1 |
20040002658 | Marian, Jr. | Jan 2004 | A1 |
20040002705 | Knowlton | Jan 2004 | A1 |
20040010222 | Nunomura et al. | Jan 2004 | A1 |
20040015079 | Berger et al. | Jan 2004 | A1 |
20040015106 | Coleman | Jan 2004 | A1 |
20040030227 | Littrup | Feb 2004 | A1 |
20040030268 | Weng et al. | Feb 2004 | A1 |
20040039312 | Hillstead | Feb 2004 | A1 |
20040039418 | Elstrom | Feb 2004 | A1 |
20040041563 | Lewin et al. | Mar 2004 | A1 |
20040041880 | Ikeda et al. | Mar 2004 | A1 |
20040042168 | Yang et al. | Mar 2004 | A1 |
20040044375 | Diederich et al. | Mar 2004 | A1 |
20040049134 | Tosaya et al. | Mar 2004 | A1 |
20040049734 | Tosaya et al. | Mar 2004 | A1 |
20040059266 | Fry | Mar 2004 | A1 |
20040068186 | Ishida et al. | Apr 2004 | A1 |
20040073079 | Altshuler et al. | Apr 2004 | A1 |
20040073113 | Salgo | Apr 2004 | A1 |
20040073115 | Horzewski et al. | Apr 2004 | A1 |
20040073116 | Smith | Apr 2004 | A1 |
20040073204 | Ryan et al. | Apr 2004 | A1 |
20040077977 | Ella et al. | Apr 2004 | A1 |
20040082857 | Schonenberger | Apr 2004 | A1 |
20040082859 | Schaer | Apr 2004 | A1 |
20040102697 | Evron | May 2004 | A1 |
20040105559 | Aylward et al. | Jun 2004 | A1 |
20040106867 | Eshel et al. | Jun 2004 | A1 |
20040122323 | Vortman et al. | Jun 2004 | A1 |
20040122493 | Ishibashi et al. | Jun 2004 | A1 |
20040143297 | Ramsey | Jul 2004 | A1 |
20040152982 | Hwang et al. | Aug 2004 | A1 |
20040158150 | Rabiner et al. | Aug 2004 | A1 |
20040186535 | Knowlton | Sep 2004 | A1 |
20040189155 | Funakubo | Sep 2004 | A1 |
20040206365 | Knowlton | Oct 2004 | A1 |
20040210214 | Knowlton | Oct 2004 | A1 |
20040217675 | Desilets | Nov 2004 | A1 |
20040249318 | Tanaka | Dec 2004 | A1 |
20040254620 | Lacoste | Dec 2004 | A1 |
20040267252 | Washington et al. | Dec 2004 | A1 |
20050007879 | Nishida | Jan 2005 | A1 |
20050033201 | Takahashi | Feb 2005 | A1 |
20050033316 | Kertz | Feb 2005 | A1 |
20050038340 | Vaezy et al. | Feb 2005 | A1 |
20050055018 | Kreindel | Mar 2005 | A1 |
20050055073 | Weber | Mar 2005 | A1 |
20050061834 | Garcia et al. | Mar 2005 | A1 |
20050070961 | Maki | Mar 2005 | A1 |
20050074407 | Smith | Apr 2005 | A1 |
20050080469 | Larson | Apr 2005 | A1 |
20050085731 | Miller et al. | Apr 2005 | A1 |
20050091770 | Mourad et al. | May 2005 | A1 |
20050096542 | Weng et al. | May 2005 | A1 |
20050104690 | Larson et al. | May 2005 | A1 |
20050113689 | Gritzky | May 2005 | A1 |
20050131302 | Poland | Jun 2005 | A1 |
20050137656 | Malak | Jun 2005 | A1 |
20050143677 | Young et al. | Jun 2005 | A1 |
20050154313 | Desilets | Jul 2005 | A1 |
20050154314 | Quistgaard | Jul 2005 | A1 |
20050154332 | Zanelli | Jul 2005 | A1 |
20050154431 | Quistgaard | Jul 2005 | A1 |
20050187495 | Quistgaard | Aug 2005 | A1 |
20050191252 | Mitsui | Sep 2005 | A1 |
20050193451 | Quistgaard | Sep 2005 | A1 |
20050193820 | Sheljaskow et al. | Sep 2005 | A1 |
20050197681 | Barolet et al. | Sep 2005 | A1 |
20050228281 | Nefos | Oct 2005 | A1 |
20050240127 | Seip et al. | Oct 2005 | A1 |
20050240170 | Zhang et al. | Oct 2005 | A1 |
20050251120 | Anderson et al. | Nov 2005 | A1 |
20050251125 | Pless et al. | Nov 2005 | A1 |
20050256406 | Barthe | Nov 2005 | A1 |
20050261584 | Eshel | Nov 2005 | A1 |
20050261585 | Makin et al. | Nov 2005 | A1 |
20050267454 | Hissong | Dec 2005 | A1 |
20050288748 | Li et al. | Dec 2005 | A1 |
20060004306 | Altshuler | Jan 2006 | A1 |
20060020260 | Dover et al. | Jan 2006 | A1 |
20060025756 | Francischelli | Feb 2006 | A1 |
20060042201 | Curry | Mar 2006 | A1 |
20060058664 | Barthe | Mar 2006 | A1 |
20060058671 | Vitek et al. | Mar 2006 | A1 |
20060058707 | Barthe | Mar 2006 | A1 |
20060058712 | Altshuler et al. | Mar 2006 | A1 |
20060074309 | Bonnefous | Apr 2006 | A1 |
20060074313 | Slayton et al. | Apr 2006 | A1 |
20060074314 | Slayton | Apr 2006 | A1 |
20060074355 | Slayton | Apr 2006 | A1 |
20060079816 | Barthe | Apr 2006 | A1 |
20060079868 | Makin | Apr 2006 | A1 |
20060084891 | Barthe | Apr 2006 | A1 |
20060089632 | Barthe | Apr 2006 | A1 |
20060089688 | Panescu | Apr 2006 | A1 |
20060094988 | Tosaya | May 2006 | A1 |
20060106325 | Perrier | May 2006 | A1 |
20060111744 | Makin | May 2006 | A1 |
20060116583 | Ogasawara et al. | Jun 2006 | A1 |
20060116671 | Slayton | Jun 2006 | A1 |
20060122508 | Slayton | Jun 2006 | A1 |
20060122509 | Desilets | Jun 2006 | A1 |
20060161062 | Arditi et al. | Jul 2006 | A1 |
20060184069 | Vaitekunas | Aug 2006 | A1 |
20060184071 | Klopotek | Aug 2006 | A1 |
20060189972 | Grossman | Aug 2006 | A1 |
20060206105 | Chopra | Sep 2006 | A1 |
20060224090 | Ostrovsky et al. | Oct 2006 | A1 |
20060229514 | Wiener | Oct 2006 | A1 |
20060238068 | May et al. | Oct 2006 | A1 |
20060241440 | Eshel | Oct 2006 | A1 |
20060241442 | Barthe | Oct 2006 | A1 |
20060241470 | Novak et al. | Oct 2006 | A1 |
20060241576 | Diederich et al. | Oct 2006 | A1 |
20060250046 | Koizumi et al. | Nov 2006 | A1 |
20060282691 | Barthe | Dec 2006 | A1 |
20060291710 | Wang et al. | Dec 2006 | A1 |
20070016039 | Vortman et al. | Jan 2007 | A1 |
20070032784 | Gilklich et al. | Feb 2007 | A1 |
20070035201 | Desilets | Feb 2007 | A1 |
20070055154 | Torbati | Mar 2007 | A1 |
20070055155 | Owen et al. | Mar 2007 | A1 |
20070055156 | Desilets et al. | Mar 2007 | A1 |
20070065420 | Johnson | Mar 2007 | A1 |
20070078290 | Esenaliev | Apr 2007 | A1 |
20070083120 | Cain et al. | Apr 2007 | A1 |
20070087060 | Dietrich | Apr 2007 | A1 |
20070088245 | Babaev et al. | Apr 2007 | A1 |
20070088346 | Mirizzi et al. | Apr 2007 | A1 |
20070161902 | Dan | Jul 2007 | A1 |
20070166357 | Shaffer et al. | Jul 2007 | A1 |
20070167709 | Slayton | Jul 2007 | A1 |
20070018553 | Kennedy | Aug 2007 | A1 |
20070208253 | Slayton | Sep 2007 | A1 |
20070219448 | Seip et al. | Sep 2007 | A1 |
20070219604 | Yaroslavsky et al. | Sep 2007 | A1 |
20070219605 | Yaroslavsky et al. | Sep 2007 | A1 |
20070238994 | Stecco et al. | Oct 2007 | A1 |
20070239075 | Rosenberg | Oct 2007 | A1 |
20070239077 | Azhari et al. | Oct 2007 | A1 |
20070239079 | Manstein et al. | Oct 2007 | A1 |
20070239142 | Altshuler | Oct 2007 | A1 |
20080015435 | Cribbs et al. | Jan 2008 | A1 |
20080027328 | Klopotek | Jan 2008 | A1 |
20080033458 | McLean et al. | Feb 2008 | A1 |
20080039724 | Seip et al. | Feb 2008 | A1 |
20080071255 | Barthe | Mar 2008 | A1 |
20080086054 | Slayton | Apr 2008 | A1 |
20080086056 | Chang et al. | Apr 2008 | A1 |
20080097214 | Meyers et al. | Apr 2008 | A1 |
20080097253 | Pedersen et al. | Apr 2008 | A1 |
20080114251 | Weymer | May 2008 | A1 |
20080139943 | Deng et al. | Jun 2008 | A1 |
20080139974 | Da Silva | Jun 2008 | A1 |
20080146970 | Litman et al. | Jun 2008 | A1 |
20080167556 | Thompson | Jul 2008 | A1 |
20080183077 | Moreau-Gobard et al. | Jul 2008 | A1 |
20080183110 | Davenport et al. | Jul 2008 | A1 |
20080188745 | Chen et al. | Aug 2008 | A1 |
20080194964 | Randall et al. | Aug 2008 | A1 |
20080195000 | Spooner et al. | Aug 2008 | A1 |
20080200810 | Buchalter | Aug 2008 | A1 |
20080200813 | Quistgaard | Aug 2008 | A1 |
20080214966 | Slayton | Sep 2008 | A1 |
20080214988 | Altshuler et al. | Sep 2008 | A1 |
20080221491 | Slayton | Sep 2008 | A1 |
20080223379 | Stuker | Sep 2008 | A1 |
20080242991 | Moon et al. | Oct 2008 | A1 |
20080243035 | Crunkilton | Oct 2008 | A1 |
20080269608 | Anderson et al. | Oct 2008 | A1 |
20080275342 | Barthe | Nov 2008 | A1 |
20080281206 | Bartlett et al. | Nov 2008 | A1 |
20080281236 | Eshel et al. | Nov 2008 | A1 |
20080281237 | Slayton | Nov 2008 | A1 |
20080281255 | Slayton | Nov 2008 | A1 |
20080294072 | Crutchfield, III | Nov 2008 | A1 |
20080294073 | Barthe | Nov 2008 | A1 |
20080319356 | Cain | Dec 2008 | A1 |
20090005680 | Jones et al. | Jan 2009 | A1 |
20090012394 | Hobelsberger et al. | Jan 2009 | A1 |
20090043198 | Milner et al. | Feb 2009 | A1 |
20090043293 | Pankratov et al. | Feb 2009 | A1 |
20090048514 | Azhari et al. | Feb 2009 | A1 |
20090069677 | Chen et al. | Mar 2009 | A1 |
20090093737 | Chomas et al. | Apr 2009 | A1 |
20090156969 | Santangelo | Jun 2009 | A1 |
20090163807 | Sliwa | Jun 2009 | A1 |
20090171252 | Bockenstedt et al. | Jul 2009 | A1 |
20090171266 | Harris | Jul 2009 | A1 |
20090177122 | Peterson | Jul 2009 | A1 |
20090177123 | Peterson | Jul 2009 | A1 |
20090182231 | Barthe et al. | Jul 2009 | A1 |
20090198157 | Babaev et al. | Aug 2009 | A1 |
20090216159 | Slayton et al. | Aug 2009 | A1 |
20090226424 | Hsu | Sep 2009 | A1 |
20090227910 | Pedersen et al. | Sep 2009 | A1 |
20090230823 | Kushculey et al. | Sep 2009 | A1 |
20090240146 | Bockenstedt | Sep 2009 | A1 |
20090253988 | Slayton et al. | Oct 2009 | A1 |
20090281463 | Chapelon et al. | Nov 2009 | A1 |
20090312693 | Thapliyal et al. | Dec 2009 | A1 |
20090318909 | Debenedictis et al. | Dec 2009 | A1 |
20090326420 | Moonen et al. | Dec 2009 | A1 |
20100011236 | Barthe et al. | Jan 2010 | A1 |
20100022919 | Peterson | Jan 2010 | A1 |
20100022921 | Seip et al. | Jan 2010 | A1 |
20100022922 | Barthe et al. | Jan 2010 | A1 |
20100030076 | Vortman et al. | Feb 2010 | A1 |
20100042020 | Ben-Ezra | Feb 2010 | A1 |
20100049178 | Deem et al. | Feb 2010 | A1 |
20100056925 | Zhang et al. | Mar 2010 | A1 |
20100056962 | Vortman et al. | Mar 2010 | A1 |
20100100014 | Eshel et al. | Apr 2010 | A1 |
20100113983 | Heckerman et al. | May 2010 | A1 |
20100130891 | Taggart et al. | May 2010 | A1 |
20100160782 | Slayton et al. | Jun 2010 | A1 |
20100160837 | Hunziker et al. | Jun 2010 | A1 |
20100168576 | Poland et al. | Jul 2010 | A1 |
20100191120 | Kraus et al. | Jul 2010 | A1 |
20100241035 | Barthe et al. | Sep 2010 | A1 |
20100249602 | Buckley et al. | Sep 2010 | A1 |
20100249669 | Ulric et al. | Sep 2010 | A1 |
20100256489 | Pedersen et al. | Oct 2010 | A1 |
20100274161 | Azhari et al. | Oct 2010 | A1 |
20100280420 | Barthe et al. | Nov 2010 | A1 |
20100286518 | Lee et al. | Nov 2010 | A1 |
20100312150 | Douglas et al. | Dec 2010 | A1 |
20110040171 | Foley et al. | Feb 2011 | A1 |
20110040190 | Jahnke et al. | Feb 2011 | A1 |
20110040213 | Dietz et al. | Feb 2011 | A1 |
20110040214 | Foley et al. | Feb 2011 | A1 |
20110066084 | Desilets et al. | Mar 2011 | A1 |
20110072970 | Slobodzian et al. | Mar 2011 | A1 |
20110077514 | Ulric et al. | Mar 2011 | A1 |
20110079083 | Yoo et al. | Apr 2011 | A1 |
20110087099 | Eshel et al. | Apr 2011 | A1 |
20110087255 | McCormack et al. | Apr 2011 | A1 |
20110112405 | Barthe et al. | May 2011 | A1 |
20110144490 | Davis et al. | Jun 2011 | A1 |
20110178444 | Slayton et al. | Jul 2011 | A1 |
20110178541 | Azhari | Jul 2011 | A1 |
20110190745 | Uebelhoer et al. | Aug 2011 | A1 |
20110201976 | Sanghvi et al. | Aug 2011 | A1 |
20110251524 | Azhari et al. | Oct 2011 | A1 |
20110251527 | Kushculey et al. | Oct 2011 | A1 |
20110270137 | Goren et al. | Nov 2011 | A1 |
20110319793 | Henrik et al. | Dec 2011 | A1 |
20110319794 | Gertner | Dec 2011 | A1 |
20120004549 | Barthe et al. | Jan 2012 | A1 |
20120016239 | Barthe et al. | Jan 2012 | A1 |
20120029353 | Slayton et al. | Feb 2012 | A1 |
20120035473 | Sanghvi et al. | Feb 2012 | A1 |
20120035475 | Barthe et al. | Feb 2012 | A1 |
20120035476 | Barthe et al. | Feb 2012 | A1 |
20120046547 | Barthe et al. | Feb 2012 | A1 |
20120053458 | Barthe et al. | Mar 2012 | A1 |
20120059288 | Barthe et al. | Mar 2012 | A1 |
20120111339 | Barthe et al. | May 2012 | A1 |
20120123304 | Rybyanets et al. | May 2012 | A1 |
20120136280 | Rosenberg et al. | May 2012 | A1 |
20120136282 | Rosenberg et al. | May 2012 | A1 |
20120143056 | Slayton et al. | Jun 2012 | A1 |
20120143100 | Jeong et al. | Jun 2012 | A1 |
20120165668 | Slayton et al. | Jun 2012 | A1 |
20120165848 | Slayton et al. | Jun 2012 | A1 |
20120191019 | Desilets et al. | Jul 2012 | A1 |
20120191020 | Vitek et al. | Jul 2012 | A1 |
20120197120 | Makin et al. | Aug 2012 | A1 |
20120197121 | Slayton et al. | Aug 2012 | A1 |
20120203108 | Tsujita | Aug 2012 | A1 |
20120209150 | Zeng et al. | Aug 2012 | A1 |
20120215105 | Slayton et al. | Aug 2012 | A1 |
20120271202 | Wisdom | Oct 2012 | A1 |
20120271294 | Barthe et al. | Oct 2012 | A1 |
20120277587 | Adanny et al. | Nov 2012 | A1 |
20120277639 | Pollock et al. | Nov 2012 | A1 |
20120296240 | Azhari et al. | Nov 2012 | A1 |
20120302883 | Kong et al. | Nov 2012 | A1 |
20120316426 | Foley et al. | Dec 2012 | A1 |
20120330197 | Makin et al. | Dec 2012 | A1 |
20120330222 | Makin et al. | Dec 2012 | A1 |
20120330223 | Makin et al. | Dec 2012 | A1 |
20120330283 | Hyde et al. | Dec 2012 | A1 |
20120330284 | Hyde et al. | Dec 2012 | A1 |
20130012755 | Slayton | Jan 2013 | A1 |
20130012816 | Slayton et al. | Jan 2013 | A1 |
20130012838 | Jaeger et al. | Jan 2013 | A1 |
20130012842 | Barthe | Jan 2013 | A1 |
20130018285 | Park et al. | Jan 2013 | A1 |
20130018286 | Slayton et al. | Jan 2013 | A1 |
20130046209 | Slayton et al. | Feb 2013 | A1 |
20130051178 | Rybyanets | Feb 2013 | A1 |
20130060170 | Lee et al. | Mar 2013 | A1 |
20130066208 | Barthe et al. | Mar 2013 | A1 |
20130066237 | Smotrich et al. | Mar 2013 | A1 |
20130072826 | Slayton et al. | Mar 2013 | A1 |
20130073001 | Campbell | Mar 2013 | A1 |
20130096471 | Slayton et al. | Apr 2013 | A1 |
20130096596 | Schafer | Apr 2013 | A1 |
20130190659 | Slayton et al. | Jul 2013 | A1 |
20130211293 | Auboiroux et al. | Aug 2013 | A1 |
20130225994 | Hsu et al. | Aug 2013 | A1 |
20130268032 | Neev | Oct 2013 | A1 |
20130274603 | Barthe et al. | Oct 2013 | A1 |
20130278111 | Sammoura | Oct 2013 | A1 |
20130281853 | Slayton et al. | Oct 2013 | A1 |
20130281891 | Slayton et al. | Oct 2013 | A1 |
20130296697 | Slayton et al. | Nov 2013 | A1 |
20130296700 | Slayton et al. | Nov 2013 | A1 |
20130296743 | Lee et al. | Nov 2013 | A1 |
20130303904 | Barthe et al. | Nov 2013 | A1 |
20130303905 | Barthe et al. | Nov 2013 | A1 |
20130310714 | Eshel et al. | Nov 2013 | A1 |
20130310863 | Makin et al. | Nov 2013 | A1 |
20130345562 | Barthe et al. | Dec 2013 | A1 |
20140024974 | Slayton et al. | Jan 2014 | A1 |
20140050054 | Toda et al. | Feb 2014 | A1 |
20140081300 | Melodelima et al. | Mar 2014 | A1 |
20140082907 | Barthe et al. | Mar 2014 | A1 |
20140117814 | Toda et al. | May 2014 | A1 |
20140142430 | Slayton et al. | May 2014 | A1 |
20140148834 | Barthe et al. | May 2014 | A1 |
20140155747 | Bennett | Jun 2014 | A1 |
20140180174 | Slayton et al. | Jun 2014 | A1 |
20140187944 | Slayton et al. | Jul 2014 | A1 |
20140188015 | Slayton et al. | Jul 2014 | A1 |
20140188145 | Slayton et al. | Jul 2014 | A1 |
20140194723 | Herzog et al. | Jul 2014 | A1 |
20140208856 | Schmid | Jul 2014 | A1 |
20140221823 | Keogh et al. | Aug 2014 | A1 |
20140236049 | Barthe et al. | Aug 2014 | A1 |
20140236061 | Lee et al. | Aug 2014 | A1 |
20140243713 | Slayton et al. | Aug 2014 | A1 |
20140257145 | Emery | Sep 2014 | A1 |
20140276055 | Barthe et al. | Sep 2014 | A1 |
20140316269 | Zhang et al. | Oct 2014 | A1 |
20150000674 | Barthe et al. | Jan 2015 | A1 |
20150025420 | Slayton et al. | Jan 2015 | A1 |
20150031995 | Guracar | Jan 2015 | A1 |
20150064165 | Perry et al. | Mar 2015 | A1 |
20150080723 | Barthe et al. | Mar 2015 | A1 |
20150080771 | Barthe et al. | Mar 2015 | A1 |
20150080874 | Slayton et al. | Mar 2015 | A1 |
20150088182 | Slayton et al. | Mar 2015 | A1 |
20150141734 | Chapelon et al. | May 2015 | A1 |
20150164734 | Slayton et al. | Jun 2015 | A1 |
20150165238 | Slayton et al. | Jun 2015 | A1 |
20150165243 | Slayton et al. | Jun 2015 | A1 |
20150174388 | Slayton | Jun 2015 | A1 |
20150202468 | Slayton et al. | Jul 2015 | A1 |
20150217141 | Barthe et al. | Aug 2015 | A1 |
20150238258 | Palero et al. | Aug 2015 | A1 |
20150297188 | Konofagou | Oct 2015 | A1 |
20150321026 | Branson et al. | Nov 2015 | A1 |
20150360058 | Barthe et al. | Dec 2015 | A1 |
20150374333 | Barthe et al. | Dec 2015 | A1 |
20150375014 | Slayton et al. | Dec 2015 | A1 |
20160001097 | Cho et al. | Jan 2016 | A1 |
20160016015 | Slayton et al. | Jan 2016 | A1 |
20160027994 | Toda et al. | Jan 2016 | A1 |
20160151618 | Powers et al. | Jun 2016 | A1 |
20160158580 | Slayton et al. | Jun 2016 | A1 |
20160175619 | Lee et al. | Jun 2016 | A1 |
20160206335 | Slayton | Jul 2016 | A1 |
20160206341 | Slayton | Jul 2016 | A1 |
20160256675 | Slayton | Sep 2016 | A1 |
20160296769 | Barthe et al. | Oct 2016 | A1 |
20160310444 | Dobak, III | Oct 2016 | A1 |
20160361571 | Bernabei | Dec 2016 | A1 |
20160361572 | Slayton | Dec 2016 | A1 |
20170028227 | Emery et al. | Feb 2017 | A1 |
20170043190 | Barthe et al. | Feb 2017 | A1 |
20170050019 | Ron Edoute et al. | Feb 2017 | A1 |
20170080257 | Paunescu et al. | Mar 2017 | A1 |
20170090507 | Weiner et al. | Mar 2017 | A1 |
20170100585 | Hall et al. | Apr 2017 | A1 |
20170119345 | Levien et al. | May 2017 | A1 |
20170136263 | Reil | May 2017 | A1 |
20170209201 | Slayton et al. | Jul 2017 | A1 |
20170209202 | Friedrichs et al. | Jul 2017 | A1 |
20170304654 | Blanche et al. | Oct 2017 | A1 |
20170368574 | Sammoura | Dec 2017 | A1 |
20180001113 | Streeter | Jan 2018 | A1 |
20180015308 | Reed et al. | Jan 2018 | A1 |
20180043147 | Slayton | Feb 2018 | A1 |
20180099162 | Bernabei | Apr 2018 | A1 |
20180099163 | Bernabei | Apr 2018 | A1 |
20180126190 | Aviad et al. | May 2018 | A1 |
20180154184 | Kong et al. | Jun 2018 | A1 |
20180177912 | Kaioptas et al. | Jun 2018 | A1 |
20180207450 | Sanchez et al. | Jul 2018 | A1 |
20180272156 | Slayton et al. | Sep 2018 | A1 |
20180272157 | Barthe et al. | Sep 2018 | A1 |
20180272158 | Barthe et al. | Sep 2018 | A1 |
20180272159 | Slayton et al. | Sep 2018 | A1 |
20180317884 | Chapelon et al. | Nov 2018 | A1 |
20180333595 | Barthe et al. | Nov 2018 | A1 |
20180360420 | Vortman et al. | Dec 2018 | A1 |
20190000498 | Barthe et al. | Jan 2019 | A1 |
20190009110 | Gross et al. | Jan 2019 | A1 |
20190009111 | Myhr et al. | Jan 2019 | A1 |
20190022405 | Greenbaum et al. | Jan 2019 | A1 |
20190038921 | Domankevitz | Feb 2019 | A1 |
20190060675 | Krone et al. | Feb 2019 | A1 |
20190091490 | Alexander et al. | Mar 2019 | A1 |
20190142380 | Emery et al. | May 2019 | A1 |
20190143148 | Slayton | May 2019 | A1 |
20190184202 | Zereshkian et al. | Jun 2019 | A1 |
20190184203 | Slayton et al. | Jun 2019 | A1 |
20190184205 | Slayton et al. | Jun 2019 | A1 |
20190184207 | Barthe et al. | Jun 2019 | A1 |
20190184208 | Barthe et al. | Jun 2019 | A1 |
20190224501 | Burdette | Jul 2019 | A1 |
20190262634 | Barthe et al. | Aug 2019 | A1 |
20190282834 | Zawada et al. | Sep 2019 | A1 |
20190290939 | Watson et al. | Sep 2019 | A1 |
20190350562 | Slayton et al. | Nov 2019 | A1 |
20190366126 | Pahk et al. | Dec 2019 | A1 |
20190366127 | Emery | Dec 2019 | A1 |
20190366128 | Slayton et al. | Dec 2019 | A1 |
20200008779 | Göksel et al. | Jan 2020 | A1 |
20200094083 | Slayton et al. | Mar 2020 | A1 |
20200100762 | Barthe et al. | Apr 2020 | A1 |
20200129759 | Schwarz | Apr 2020 | A1 |
20200171330 | Barthe et al. | Jun 2020 | A1 |
20200179727 | Slayton et al. | Jun 2020 | A1 |
20200179729 | Slayton et al. | Jun 2020 | A1 |
20200188703 | Barthe et al. | Jun 2020 | A1 |
20200188704 | Barthe et al. | Jun 2020 | A1 |
20200188705 | Emery et al. | Jun 2020 | A1 |
20200206072 | Capelli et al. | Jul 2020 | A1 |
20200222728 | Khokhlova et al. | Jul 2020 | A1 |
20210038925 | Emery | Feb 2021 | A1 |
20210378630 | Slayton et al. | Dec 2021 | A1 |
Number | Date | Country |
---|---|---|
2460061 | Nov 2001 | CN |
1734284 | Dec 2009 | CN |
102112059 | Jun 2011 | CN |
102573648 | Jul 2012 | CN |
104027893 | Sep 2014 | CN |
106994041 | Aug 2017 | CN |
108023552 | May 2018 | CN |
4029175 | Mar 1992 | DE |
10140064 | Mar 2003 | DE |
10219297 | Nov 2003 | DE |
10219217 | Dec 2004 | DE |
20314479 | Dec 2004 | DE |
0142215 | May 1984 | EP |
0344773 | Dec 1989 | EP |
0473553 | Apr 1992 | EP |
670147 | Feb 1995 | EP |
0661029 | Jul 1995 | EP |
724894 | Feb 1996 | EP |
763371 | Nov 1996 | EP |
1044038 | Oct 2000 | EP |
1050322 | Nov 2000 | EP |
1234566 | Aug 2002 | EP |
1262160 | Dec 2002 | EP |
1283690 | Feb 2003 | EP |
0659387 | Apr 2003 | EP |
1374944 | Jan 2004 | EP |
1479412 | Nov 2004 | EP |
1028660 | Jan 2008 | EP |
1874241 | Jan 2008 | EP |
1362223 | May 2008 | EP |
1750804 | Jul 2008 | EP |
1811901 | Apr 2009 | EP |
1785164 | Aug 2009 | EP |
2230904 | Sep 2010 | EP |
1501331 | Jun 2011 | EP |
2066405 | Nov 2011 | EP |
2474050 | Jul 2012 | EP |
2527828 | Nov 2012 | EP |
2897547 | Jul 2015 | EP |
2709726 | Nov 2015 | EP |
1538980 | Jan 2017 | EP |
3124047 | Jan 2017 | EP |
2173261 | Aug 2018 | EP |
3417911 | Dec 2018 | EP |
2532851 | Sep 1983 | FR |
2685872 | Jan 1992 | FR |
2672486 | Aug 1992 | FR |
2703254 | Mar 1994 | FR |
2113099 | Aug 1983 | GB |
102516 | Jan 1996 | IL |
112369 | Aug 1999 | IL |
120079 | Mar 2001 | IL |
63036171 | Feb 1988 | JP |
03048299 | Mar 1991 | JP |
3123559 | May 1991 | JP |
03136642 | Jun 1991 | JP |
4089058 | Mar 1992 | JP |
04150847 | May 1992 | JP |
7080087 | Mar 1995 | JP |
07505793 | Jun 1995 | JP |
7184907 | Jul 1995 | JP |
7222782 | Aug 1995 | JP |
09047458 | Feb 1997 | JP |
9108288 | Apr 1997 | JP |
9503926 | Apr 1997 | JP |
3053069 | Oct 1998 | JP |
11123226 | May 1999 | JP |
11505440 | May 1999 | JP |
11506636 | Jun 1999 | JP |
10248850 | Sep 1999 | JP |
2000126310 | May 2000 | JP |
2000166940 | Jun 2000 | JP |
2000233009 | Aug 2000 | JP |
2001-46387 | Feb 2001 | JP |
2001136599 | May 2001 | JP |
2001170068 | Jun 2001 | JP |
2002505596 | Feb 2002 | JP |
2002078764 | Mar 2002 | JP |
2002515786 | May 2002 | JP |
2002537013 | May 2002 | JP |
2002521118 | Jul 2002 | JP |
2002537939 | Nov 2002 | JP |
2003050298 | Jul 2003 | JP |
2003204982 | Jul 2003 | JP |
2004-504898 | Feb 2004 | JP |
2004-507280 | Mar 2004 | JP |
2004154256 | Mar 2004 | JP |
2004-509671 | Apr 2004 | JP |
2004-512856 | Apr 2004 | JP |
2004130145 | Apr 2004 | JP |
2004147719 | May 2004 | JP |
2005503388 | Feb 2005 | JP |
2005527336 | Sep 2005 | JP |
2005323213 | Nov 2005 | JP |
2006520247 | Sep 2006 | JP |
2008515559 | May 2008 | JP |
2009518126 | May 2009 | JP |
2010517695 | May 2010 | JP |
2001-0019317 | Mar 2001 | KR |
1020010024871 | Mar 2001 | KR |
2002-0038547 | May 2002 | KR |
100400870 | Oct 2003 | KR |
1020060113930 | Nov 2006 | KR |
1020070065332 | Jun 2007 | KR |
1020070070161 | Jul 2007 | KR |
1020070098856 | Oct 2007 | KR |
1020000059516 | Apr 2012 | KR |
10-1365946 | Feb 2014 | KR |
386883 | Sep 2000 | TW |
201208734 | Mar 2012 | TW |
WO9312742 | Jul 1993 | WO |
WO9524159 | Sep 1995 | WO |
WO9625888 | Aug 1996 | WO |
WO9634568 | Nov 1996 | WO |
WO9639079 | Dec 1996 | WO |
WO9735518 | Oct 1997 | WO |
WO9832379 | Jul 1998 | WO |
WO9852465 | Nov 1998 | WO |
WO9933520 | Jul 1999 | WO |
WO9939677 | Aug 1999 | WO |
WO9949788 | Oct 1999 | WO |
WO200006032 | Feb 2000 | WO |
WO0015300 | Mar 2000 | WO |
WO0021612 | Apr 2000 | WO |
WO0048518 | Aug 2000 | WO |
WO0053113 | Sep 2000 | WO |
WO200071021 | Nov 2000 | WO |
WO0128623 | Apr 2001 | WO |
WO01045550 | Jun 2001 | WO |
WO0182777 | Nov 2001 | WO |
WO0182778 | Nov 2001 | WO |
WO0187161 | Nov 2001 | WO |
WO01080709 | Nov 2001 | WO |
WO2001087161 | Nov 2001 | WO |
WO0209812 | Feb 2002 | WO |
WO0209813 | Feb 2002 | WO |
WO02015768 | Feb 2002 | WO |
WO0224050 | Mar 2002 | WO |
WO200149194 | Jul 2002 | WO |
WO2002054018 | Jul 2002 | WO |
WO02092168 | Nov 2002 | WO |
WO03053266 | Jul 2003 | WO |
WO03065347 | Aug 2003 | WO |
WO03070105 | Aug 2003 | WO |
WO03077833 | Sep 2003 | WO |
WO03086215 | Oct 2003 | WO |
WO03096883 | Nov 2003 | WO |
WO03099177 | Dec 2003 | WO |
WO03099382 | Dec 2003 | WO |
WO03101530 | Dec 2003 | WO |
WO2004000116 | Dec 2003 | WO |
WO2004080147 | Sep 2004 | WO |
WO2004110558 | Dec 2004 | WO |
WO2005011804 | Feb 2005 | WO |
WO2005065408 | Jul 2005 | WO |
WO2005065409 | Jul 2005 | WO |
WO2005090978 | Sep 2005 | WO |
WO2005113068 | Dec 2005 | WO |
WO2006042163 | Apr 2006 | WO |
WO2006036870 | Apr 2006 | WO |
WO2006042168 | Apr 2006 | WO |
WO2006042201 | Apr 2006 | WO |
WO2006065671 | Jun 2006 | WO |
WO2006082573 | Aug 2006 | WO |
WO2006104568 | Oct 2006 | WO |
WO2006110388 | Oct 2006 | WO |
WO2007067563 | Jun 2007 | WO |
WO2008036479 | Mar 2008 | WO |
WO2008036622 | Mar 2008 | WO |
WO2008144274 | Nov 2008 | WO |
WO2009013729 | Jan 2009 | WO |
WO2009149390 | Dec 2009 | WO |
WO2010006293 | Jan 2010 | WO |
WO2010102128 | Sep 2010 | WO |
WO2012134645 | Oct 2012 | WO |
WO2013048912 | Apr 2013 | WO |
WO2013178830 | Dec 2013 | WO |
WO2014043206 | Mar 2014 | WO |
WO2014045216 | Mar 2014 | WO |
WO2014055708 | Apr 2014 | WO |
WO2014057388 | Apr 2014 | WO |
WO2014127091 | Aug 2014 | WO |
WO 2014137835 | Sep 2014 | WO |
WO2015160708 | Oct 2015 | WO |
WO2016054155 | Apr 2016 | WO |
WO2016115363 | Jul 2016 | WO |
WO2017127328 | Jul 2017 | WO |
WO2017149506 | Sep 2017 | WO |
WO2017165595 | Sep 2017 | WO |
WO2017212489 | Dec 2017 | WO |
WO2017223312 | Dec 2017 | WO |
WO2018035012 | Feb 2018 | WO |
WO2018158355 | Sep 2018 | WO |
WO2019008573 | Jan 2019 | WO |
WO 2019147596 | Aug 2019 | WO |
WO2019164836 | Aug 2019 | WO |
WO2020009324 | Jan 2020 | WO |
WO2020075906 | Apr 2020 | WO |
WO2020080730 | Apr 2020 | WO |
WO2020121307 | Jun 2020 | WO |
WO2022240843 | Nov 2022 | WO |
Entry |
---|
US 10,398,895 B2, 09/2019, Schwarz (withdrawn) |
Adams et al., “High Intensity Focused Ultrasound Ablation of Rabbit Kidney Tumors”Sonablate High-Intensity Focused Ultrasound device; Journal of Endourology vol. 10, No. 1, (Feb. 1996). |
Agren, Magnus S. et al., Collagenase in Wound Healing: Effect of Wound Age and Type. The Journal of Investigative Dermatology, vol. 99/No. 6, (Dec. 1992). |
Alam, M., “The future of noninvasive procedural dermatology”. Semin Cutan Med Surg. Mar. 2013; 32(1):59-61. |
Alam, M., et al., “Ultrasound tightening of facial and neck skin: a rater-blinded prospective cohort study”. J Am Acad Dermatol, 2010. 62(2): p. 262-9. |
Alexiades-Armenakas, M., “Ultrasound Technologies for Dermatologic Techniques”. J Drugs Derm. 2014. 12 (11): p. 1305. |
Alster, T.S., et al., “Noninvasive lifting of arm, thigh, and knee skin with transcutaneous intense focused ultrasound”. Dermatol Surg, 2012. 38(5): p. 754-9. |
Alster, Tinas S., Tanzi, Elizabeth L., “Cellulite Treatment using a Novel CombinationRadiofrequency, Infrared Light, and Mechanical Tissue Manipulation Device,” Journal of Cosmetic & Laser Therapy, Jun. 2005, vol. 7, Issue 2, pp. 81-85. |
Arosarena, O., “Options and Challenges for Facial Rejuvenation in Patients With Higher Fitzpatrick Skin Phototypes”. JAMA Facial Plastic Surgery, 2015. |
Arthur et al., “Non-invasive estimation of hyperthermia temperatures with ultrasound,” Int. J. Hyperthermia, Sep. 2005, 21(6), pp. 589-600. |
Barthe et al., “Ultrasound therapy system and ablation results utilizing miniatureimaging/therapy arrays,” Ultrasonics Symposium, 2004 IEEE, Aug. 23, 2004, pp. 1792-1795, vol. 3. |
Bozec, Laurent et al., Thermal Denaturation Studies of Collagen by MicrothermalAnalysis and Atomic Force Microscopy, Biophysical Journal, vol. 101, pp. 228-236. (Jul. 2001). |
Brobst, R.W., et al., “Noninvasive Treatment of the Neck”. Facial Plast Surg Clin North Am, 2014. 22(2): p. 191-202. |
Brobst, R.W., et., al., “Ulthera: initial and six month results”. Facial Plast Surg Clin North Am, 2012. 20(2): p. 163-76. |
Brown J A et al: “Fabrication and performance of 40-60 MHz annular arrays”, 2003 IEEE Ultrasonics Symposium Proceedings. Honolulu, Hawaii, Oct. 5-8, 2003; [IEEE Ultrasonics Symposium Proceedings], New York, NY : IEEE, US, vol. 1, Oct. 5, 2003 (Oct. 5, 2003), pp. 869-872. |
Calderhead et al., “One Mechanism Behind LED Photo-Therapy for Wound Healing and Skin Rejuvenation: Key Role of the Mast Cell” Laser Therapy 17.3: 141-148 (2008). |
Carruthers et al., “Consensus Recommendations for Combined Aesthetic Interventionsin the Face Using Botulinum Toxin, Fillers, and Energy-Based Devices” Dermatol Surg 2016 (pp. 1-12). |
Casabona, G., et al., “Microfocused Ultrasound with Visualization and CalciumHydroxylapatite for Improving Skin Laxity and Cellulite Appearance”; Plast Reconstr Surg Glob Open. Jul. 25, 2017;5(7):e1388, 8 pages. |
Casabona, G., et al., “Microfocused Ultrasound With Visualization and Fillers for Increased Neocollagenesis: Clinical and Histological Evaluation”. Dermatol Surg 2014;40:S194-S198. |
Chan, N.P., et al., “Safety study of transcutaneous focused ultrasound for non-invasive skin tightening in Asians”. Lasers Surg Med, 2011. 43(5): p. 366-75. |
Chapelon et al., “Effects of Cavitation In the High Intensity Therapeutic Ultrasound”, Ultrasonics Symposium—1357 (1991). |
Chapelon, et al., “Thresholds for Tissue Ablation by Focused Ultrasound” (1990). |
Chen, L. et al., “Effect of Blood Perfusion on the ablation of liver parenchyma with high intensity focused ultrasound,” Phys. Med. Biol; 38:1661-1673; 1993b. |
Coon, Joshua et al., “Protein identification using sequential ion/ion reactions and tandemmass spectrometry” Proceedings of the National Academy of Sciences of the USA, vol. 102, No. 27, Jul. 27, 2005, pp. 9463-9468. |
Corry, Peter M., et al., “Human Cancer Treatment with Ultrasound”, IEEE Transactions on Sonics and Ultrasonics, vol. SU-31, No. 5, Sep. 1984, pp. 444, 456. |
Damianou et al., “Application of the Thermal Dose Concept for Predicting the NecrosedTissue vol. During Ultrasound Surgery,” 1993 IEEE Ultrasound Symposium, pp. 1199-1202. |
Daum et al., Design and Evaluation of a Feedback Based Phased Array System forUltrasound Surgery, IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, vol. 45, No. 2, Mar. 1998, pp. 431-438. |
Davis, Brian J., et al., “An Acoustic Phase Shift Technique for the Non-InvasiveMeasurement of Temperature Changes in Tissues”, 1985 Ultrasonics Symposium, pp. 921-924. |
Dayan, S.H., et al., “Prospective, Multi-Center, Pivotal Trial Evaluating the Safety and Effectiveness of Micro-Focused Ultrasound with Visualization (MFU-V) for Improvement in Lines and Wrinkles of the Decolletage”. Plast Reconstr Surg. Oct. 2014; 134(4 Suppl 1):123-4. |
Decision of the Korean Intellectual Property Tribunal dated Jun. 28, 2013 regarding Korean Patent No. 10-1142108, which is related to the pending application and/or an application identified in the Table on pp. 1-4 of the Information Disclosure Statement herein (English translation, English translation certification, and Korean decision included). |
Delon Martin, C., et al., “Venous Thrombosis Generation By Means of High-Intensity Focused Ultrasound” Ultrasound in Med. & Biol., vol. 21, No. 1, pp. 113-119 (1995). |
Dierickx, Christine C., “The Role of Deep Heating for Noninvasive Skin Rejuvenation” Lasers in Surgery and Medicine 38:799-807 (2006). |
Dobke, M.K., et al., “Tissue restructuring by energy-based surgical tools”. Clin Plast Surg, 2012. 39(4): p. 399-408. |
Dong, Yuan-Lin et al., “Effect of Ibuprofen on the Inflammatory Response to Surgical Wounds” The Journal of Trauma, vol. 35, No. 3. (1993). |
Driller et al., “Therapeutic Applications of Ultrasound: A Review” IEEE Engineering in Medicine and Biology; (Dec. 1987) pp. 33-40. |
Dvivedi, Sanjay, et al. “Effect of Ibuprofen and diclofenac sodium on experimental wound healing” Indian Journal of Experimental Biology, vol. 35, pp. 1243-1245. (Nov. 1997). |
Fabi, S.G., “Microfocused Ultrasound With Visualization for Skin Tightening and Lifting: My Experience and a Review of the Literature”. Dermatol Surg. Dec. 2014; 40 Suppl 12:S164-7. |
Fabi, S.G., “Noninvasive skin tightening: focus on new ultrasound techniques”. Clin Cosmet Investig Dermatol. Feb. 5, 2015; 8:47-52. |
Fabi, S.G., et al., “A prospective multicenter pilot study of the safety and efficacy ofmicrofocused ultrasound with visualization for improving lines and wrinkles of the décolleté”. Dermatol Surg. Mar. 2015; 41(3):327-35. |
Fabi, S.G., et al., “Evaluation of microfocused ultrasound with visualization for lifting,tightening, and wrinkle reduction of the decolletage”. J Am Acad Dermatol, 2013. 69(6): p. 965-71. |
Fabi, S.G., et al., “Future directions in cutaneous laser surgery”. Dermatol Clin, 2014. 32(1): p. 61-9. |
Fabi, S.G., et al., “Retrospective Evaluation of Micro-focused Ultrasound for Lifting and Tightening the Face and Neck”. Dermatol Surg, 2014. |
Friedmann D.P., “Comments on evaluation of microfocused ultrasound system forimproving skin laxity and tightening in the lower face”. Aesthet Surg J. Mar. 2015;35(3):NP81-2. |
Friedmann, D.P., et al., “Combination of intense pulsed light, Sculptra, and Ultherapy for treatment of the aging face”. J Cosmet Dermatol, 2014. 13(2): p. 109-18. |
Fry, W.J. et al., “Production of Focal Destructive Lesions in the Central Nervous System with Ultrasound,” J. Neurosurg., 11:471-478; 1954. |
Fujimoto, et al., “A New Cavitation Suppression Technique for Local Ablation Using High-Intensity Focused Ultrasound” Ultrasonics Symposium—1629 (1995). |
Gliklich et al., Clinical Pilot Study of Intense Ultrasound therapy to Deep Dermal Facial Skin and Subcutaneous Tissues, Arch Facial Plastic Surgery, Mar. 1, 2007, vol. 9, No. 1. |
Gold, M.H., et al., “Use of Micro-Focused Ultrasound with Visualization to Lift and Tighten Lax Knee Skin”. J Cosmet Laser Ther, 2014: p. 1-15. |
Goldberg, D.J., et al., “Safety and Efficacy of Microfocused Ultrasound to Lift, Tighten, and Smooth the Buttocks”. Dermatol Surg 2014; 40:1113-1117. |
Greene, R.M., et al., “Skin tightening technologies”. Facial Plast Surg. Feb. 2014; 30(1):62-7. |
Greenhalgh, David G., “Wound healing and diabetes mellitus” Clinics in Plastic Surgery 30; 37-45. (2003). |
Guo, S. et al., “Factors Affecting Wound Healing” Critical Reviews in Oral Biology & Medicine, J Dent Res 89(3), pp. 219-229. (2010). |
Haar, G.R. et al., “Tissue Destruction with Focused Ultrasound in Vivo,” Eur. Urol. 23 (suppl. 1):8-11; 1993. |
Hantash, Basil M. et al., “Bipolar Fractional Radiofrequency Treatment Induces Neoelastogenesis and Neocollagenesis” Lasers in Surgery and Medicine 41:1-9 (2009). |
Hantash, Basil M. et al., “In Vivo Histological Evaluation of a Novel Ablative Fractional Resurfacing Device” Lasers in Surgery and Medicine 39:96-107 (2007). |
Harris, M.O., “Safety of Microfocused Ultrasound With Visualization in Patients With Fitzpatrick Skin Phototypes III to VI”. Jama Facial Plast. Surg, 2015. |
Hart, et al., “Current Concepts in the Use of PLLA: Clinical Synergy Noted with CombinedUse of Microfocused Ultrasound and Poly-I-Lactic Acid on the Face, Neck, and Décolletage”. Amer. Soc. Plast. Surg. 2015. 136; 180-187S. |
Hassan et al., “Structure and Applications of Poly(vinyl alcohol) Hydrogels Produced byConventional Crosslinking or by Freezing/Thawing Methods,” advanced in Polymer Science, 2000, pp. 37-65, vol. 153. |
Hassan et al., “Structure and Morphology of Freeze/Thawed PVA Hydrogels,” Macromolecules, Mar. 11, 2000, pp. 2472-2479, vol. 33, No. 7. |
Hexsel et al., “A Validated Photonumeric Cellulite Severity Scale”; J Eur Acad Dermatol Venereol. May 2009; 23(5):523-8, 6 pages. |
Hitchcock, T.M. et al., “Review of the safety profile for microfocused ultrasound with Visualization”. Journal of Cosmetic Dermatology, 13, 329-335. (2014). |
Husseini et al., “The Role of Cavitation in Acoustically Activated Drug Delivery,” J. Control Release, Oct. 3, 2005, pp. 253-261, vol. 107(2). |
Husseini et al. “Investigating the mechanism of acoustically activated uptake of drugs from Pluronic micelles,” BMD Cancer 2002, 2:20k, Aug. 30, 2002, pp. 1-6. |
Hynynen et al., Temperature Distributions During Local Ultrasound Induced Hyperthermia In Vivo, Ultrasonics Symposium—745 (1982). |
Jeffers et al., “Evaluation of the Effect of Cavitation Activity on Drug-Ultrasound Synergisms,” 1993 IEEE Ultrasonics Symposium, pp. 925-928. |
Jenne, J., et al., “Temperature Mapping for High Energy US-Therapy”, 1994 Ultrasonics Symposium, pp. 1879-1882. |
Jeong, K.H., et al., “Neurologic complication associated with intense focused ultrasound”. J Cosmet Laser Ther, 2013. |
Johnson, S.A., et al., “Non-Intrusive Measurement of Microwave and Ultrasound-InducedHyperthermia by Acoustic Temperature Tomography”, Ultrasonics Symposium Proceedings, pp. 977-982. (1977). |
Ketterling J. A. et al.: “Design and fabrication of a 40-MHz annular array transducer”,IEEE Transactions on Ultrasonics, Ferroelectrics and Frequency Control, IEEE, US, vol. 52, No. 4, Apr. 1, 2005 (Apr. 1, 2005), pp. 672-681. |
Kim, H.J., et al., “Coagulation and ablation patterns of high-intensity focused ultrasound on a tissue mimicking phantom and cadaveric skin”. Laser Med Sci. Sep. 4, 2015. |
Kornstein, A.N., “Ulthera for silicone lip correction”. Plast Reconstr Surg, 2012. 129(6): p. 1014e-1015e. |
Kornstein, A.N., “Ultherapy shrinks nasal skin after rhinoplasty following failure of conservative measures”. Plast Reconstr Surg, 2013. 131(4): p. 664e-6e. |
Krischak, G.D., et al., “The effects of non-steroidal anti-inflammatory drug application on incisional wound healing in rats” Journal of Wound Care, vol. 6, No. 2, (Feb. 2007). |
Laubach, H.J., et al., “Confined Thermal Damage with Intense Ultrasound (IUS)” [abstr.] American Society for Laser Medicine and Surgery Abstracts, p. 15 #43 (Apr. 2006). |
Laubach, H.J., et al., “Intense focused ultrasound: evaluation of a new treatment modality for precise microcoagulation within the skin”. Dermatol Surg, 2008. 34(5): p. 727-34. |
Lee, H.J., et al., “The efficacy and safety of intense focused ultrasound in the treatment of enlarged facial pores in Asian skin”. J Dermatolog Treat, 2014. |
Lee, H.S., et al., “Multiple Pass Ultrasound Tightening of Skin Laxity of the Lower Face and Neck”. Dermatol Surg, 2011. |
Lin, Sung-Jan, et al., “Monitoring the thermally induced structural transitions of collagen byuse of second-harmonic generation microscopy” Optics Letters, vol. 30, No. 6, (Mar. 15, 2005). |
MacGregor J.L., et al., “Microfocused Ultrasound for Skin Tightening”. Semin Cutan Med Surg 32:18-25. (2013). |
Madersbacher, S. et al., “Tissue Ablation in Benign Prostatic Hyperplasia with High Intensity Focused Ultrasound,” Dur. Urol., 23 (suppl. 1):39-43; 1993. |
Makin et al., “B-Scan Imaging and Thermal Lesion Monitoring Using Miniaturized Dual-Functionality Ultrasound Arrays,” Ultrasonics Symposium, 2004 IEEE, Aug. 23, 2004, pp. 1788-1791, vol. 3. |
Makin et al., “Confirmed Bulk Ablation and Therapy Monitoring Using Intracorporeal Image-Treat Ultrasound Arrays,” 4th International Symposium on Therapeutic Ultrasound, Sep. 19, 2004. |
Makin et al., “Miniaturized Ultrasound Arrays for Interstitial Ablation and Imaging,” UltraSound Med. Biol. 2005, Nov. 1, 2005, pp. 1539-1550, vol. 31(11). |
Manohar et al., “Photoacoustic mammography laboratory prototype: imaging of breasttissue phantoms,” Journal of Biomedical Optics, Nov./Dec. 2004, pp. 1172-1181, vol. 9, No. 6. |
Mast et al., “Bulk Ablation of Soft Tissue with Intense Ultrasound; Modeling and Experiments,” J. Acoust. Soc. Am., Oct. 1, 2005, pp. 2715-2724, vol. 118(4). |
Meshkinpour, Azin, et al., “Treatment of Hypertrophic Scars and Keloids With aRadiofrequency Device: A Study of Collagen Effects” Lasers in Surgery and Medicine 37:343-349 (2005). |
Microchip microID 125 kHz RFID System Design Guide, Microchip Technology Inc. (2004). |
Minkis, K., et al., “Ultrasound skin tightening”. Dermatol Clin, 2014. 32(1): p. 71-7. |
Mitragotri, S., “Healing sound: the use of ultrasound in drug delivery and other therapeutic applications,” Nature Reviews; Drug Delivery, pp. 255-260, vol. 4 (Mar. 2005). |
Mosser, David M. et al., “Exploring the full spectrum of macrophage activation” Nat Rev Immunol; 8(12): 958-969. (Dec. 2008). |
Murota, Sei-Itsu, et al., “Stimulatory Effect of Prostaglandins on the Production of Hexosamine-Containing Substances by Cultured Fibroblasts (3) Induction of Hyaluronic Acid Synthetase by Prostaglandin” Department of Pharmacology, Tokyo Metropolitan Institute of Gerontology, Itabashiku, Tokyo—173, Japan. (Nov. 1977, vol. 14, No. 5). |
Murota, Sei-Itsu, et al., “The Stimulatory Effect of Prostaglandins on Production of Hexosamine-Containing Substances by Cultured Fibroblasts” Department of Pharmacology, Tokyo Metropolitan Institute of Gerontology, Itabashiku, Tokyo—173, Japan. (Aug. 1976, vol. 12, No. 2). |
Narayanasamy et al., “Spatial registration of temporally separated whole breast 3Dultrasound images” Med Phys. Sep. 2009;36(9):4288-300. doi: 10.1118/1.3193678. PMID: 19810503; PMCID: PMC2749445 (2009). |
Nestor, M.S. et al., “Safety and Efficacy of Micro-focused Ultrasound Plus Visualization for the Treatment of Axillary Hyperhidrosis”. J Clin Aesthet Dermatol, 2014. 7(4): p. 14-21. |
Oni, G., et al. “Response to ‘comments on evaluation of microfocused ultrasound system forimproving skin laxity and tightening in the lower face’”. Aesthet Surg J. Mar. 2015;35(3):NP83-4. |
Oni, G., et al., “Evaluation of a Microfocused Ultrasound System for Improving Skin Laxity and Tightening in the Lower Face”. Aesthet Surg J, 2014. 38:861-868. |
Pak, C.S., et al., “Safety and Efficacy of Ulthera in the Rejuvenation of Aging Lower Eyelids: A Pivotal Clinical Trial”. Aesthetic Plast Surg, 2014. |
Paradossi et al., “Poly(vinyl alcohol) as versatile biomaterial for potential biomedicalapplications,” Journal of Materials Science: Materials in Medicine, 2003, pp. 687-691, vol. 14. |
Pritzker, R.N., et al., “Updates in noninvasive and minimally invasive skin tightening”. Semin Cutan Med Surg. Dec. 2014;33(4):182-7. |
Pritzker, R.N., et al., “Comparison of different technologies for noninvasive skin tightening”. Journal of Cosmetic Dermatology, 13, 315-323. (2014). |
Rappolee, Daniel A., et al., “Wound Macrophages Express TGF and Other GrowthFactors in Vivo: Analysis by mRNA Phenotyping” Science, vol. 241, No. 4866 (Aug. 1988). |
Reid, Gavin, et al., “Tandem Mass spectrometry of ribonuclease A and B: N-linkedglycosylation site analysis of whole protein ions,” Analytical Chemistry. Feb. 1, 2002, vol. 74, No. 3, pp. 577-583. |
Righetti et al., “Elastographic Characterization of HIFU-Induced Lesions in Canine Livers,” 1999, Ultrasound in Med & Bio, vol. 25, No. 7, pp. 1099-1113. |
Rokhsar, C., et al., “Safety and efficacy of microfocused ultrasound in tightening of lax elbow skin”. Dermatol Surg. 2015; 41(7):821-6. |
Rosenberg, Carol S. “Wound Healing in the Patient with Diabetes Mellitus” Nursing Clinics of North America, vol. 25, No. 1, (Mar. 1990). |
Saad et al., “Ultrasound-Enhanced Effects of Adriamycin Against Murine Tumors,” Ultrasound in Med. & Biol. Vol. 18, No. 8, pp. 715-723 (1992). |
Sabet-Peyman, E.J. et al., “Complications Using Intense Ultrasound Therapy to Treat Deep Dermal Facial Skin and Subcutaneous Tissues”. Dermatol Surg 2014; 40:1108-1112. |
Sandulache, Vlad C. et al., “Prostaglandin E2 inhibition of keloid fibroblast migration,contraction, and transforming growth factor (TGF)-B1-induced collagen synthesis” Wound Rep Reg 15 122-133, 2007. (2007). |
Sanghvi, N.T., et al., “Transrectal Ablation of Prostate Tissue Using Focused Ultrasound,” 1993 Ultrasonics Symposium, IEEE, pp. 1207-1210. |
Sasaki, G.H. et al., “Clinical Efficacy and Safety of Focused-Image Ultrasonography: A 2-Year Experience”. Aesthet Surg J, 2012. |
Sasaki, G.H. et al., “Microfocused Ultrasound for Nonablative Skin and Subdermal Tightening to the Periorbitum and Body Sites: Preliminary Report on Eighty-Two Patients”. Journal of Cosmetics, Dermatological Sciences and Applications, 2012, 2, 108-116. |
Sassen, Sander, “ATI's R520 architecture, the new king of the hill?” http://www.hardwareanalysis.com/content/article/1813, Sep. 16, 2005, 2 pages. |
Seip, Ralf, et al., “Noninvasive Detection of Thermal Effects Due to Highly Focused Ultrasonic Fields,” IEEE Symposium, pp. 1229-1232, vol. 2, Oct. 3-Nov. 1993. |
Seip, Ralf, et al., “Noninvasive Estimation of Tissue Temperature Response to HeatingFields Using Diagnostic Ultrasound,” IEEE Transactions on Biomedical Engineering, vol. 42, No. 8, Aug. 1995, pp. 828-839. |
Simon et al., “Applications of Lipid-Coated Microbubble Ultrasonic Contrast to Tumor Therapy,” Ultrasound in Med. & Biol. Vol. 19, No. 2, pp. 123-125 (1993). |
Sklar, L.R., et al., “Use of transcutaneous ultrasound for lipolysis and skin tightening: a review”. Aesthetic Plast Surg, 2014. 38(2): p. 429-41. |
Smith, Nadine Barrie, et al., “Non-invasive In Vivo Temperature Mapping of UltrasoundHeating Using Magnetic Resonance Techniques”, 1994 Ultrasonics Symposium, pp. 1829-1832, vol. 3. |
Sonocare, Inc. Therapeutic Ultrasound System Model CST-100 Instruction Manual (1985). |
Suh, D.H., et al., “A intense-focused ultrasound tightening for the treatment of infraorbital laxity”. J Cosmet Laser Ther, 2012. 14(6): p. 290-5. |
Suh, D.H., et al., “Comparative histometric analysis of the effects of high-intensity focused ultrasound and radiofrequency on skin”. J Cosmet Laser Ther. Mar. 24, 2015:1-7. |
Suh, D.H., et al., “Intense Focused Ultrasound Tightening in Asian Skin: Clinical and Pathologic Results” American Society for Dermatologic Surgery, Inc.; 37:1595-1602. (2011). |
Surry et al., “Poly(vinyl alcohol) cryogel phantoms for use in ultrasound and MR imaging,” Phys. Med. Biol., Dec. 6, 2004, pp. 5529-5546, vol. 49. |
Syka J. E. P. et al., “Peptide and Protein Sequence Analysis by Electron Transfer Dissociation Mass Spectrometry,” Proceedings of the National Academy of Sciences of USA, National Academy of Science, Washington, DC, vol. 101, No. 26, Jun. 29, 2004, pp. 9528-9533. |
Talbert, D. G., “An Add-On Modification for Linear Array Real-Time Ultrasound Scanners to Produce 3D Displays,” UTS Int'l 1977 Brighton, England (Jun. 28-30, 1977) pp. 57-67. |
Tata et al., “Interaction of Ultrasound and Model Membrane Systems: Analyses and Predictions,” American Chemical Society, Phys. Chem. 1992, 96, pp. 3548-3555. |
Ueno, S., et al., “Ultrasound Thermometry in Hyperthermia”, 1990 Ultrasonic Symposium, pp. 1645-1652. |
Verhofstad, Michiel H.J. et al., “Collagen Synthesis in rat skin and ileum fibroblasts is affected differently by diabetes-related factors” Int. J. Exp. Path. (1998), 79, 321-328. |
Wang, H., et al., “Limits on Focused Ultrasound for Deep Hyperthermia”, 1994 Ultrasonic Symposium, Nov. 1-4, 1994, pp. 1869-1872, vol. 3. |
Wasson, Scott, “NVIDIA's GeForce 7800 GTX graphics processor Power MADD,” http://techreport.com/reviews/2005q2/geforce-7800gtx/index.x?pg=1, Jun. 22, 2005, 4 pages. |
Webster et al. “The role of ultrasound-induced cavitation in the ‘in vitro’ stimulation of collagen synthesis in human fibroblasts”; Ultrasonics pp. 33-37(Jan. 1980). |
Weiss, M., “Commentary: noninvasive skin tightening: ultrasound and other technologies: where are we in 2011?” Dermatol Surg, 2012. 38(1): p. 28-30. |
White et al.“Selective Creating of Thermal Injury Zones in the Superficial Musculoaponeurotic System Using Intense Ultrasound Therapy,” Arch Facial Plastic Surgery, Jan./Feb. 2007, vol. 9, No. 1 (pp. 22-29). |
White, W. M., et al., “Selective Transcutaneous Delivery of Energy to Facial SubdermalTissues Using the Ultrasound Therapy System” [abstr]. American Society for Laser Medicine and Surgery Abstracts, p. 37 #113 (Apr. 2006). |
White, W. Matthew, et al., “Selective Transcutaneous Delivery of Energy to Porcine Soft Tissues Using Intense Ultrasound (IUS)” Lasers in Surgery and Medicine 40:67-75 (2008). |
Woodward, J.A., et al. “Safety and Efficacy of Combining Microfocused Ultrasound WithFractional CO2 Laser Resurfacing for Lifting and Tightening the Face and Neck”. Dermatol Surg, Dec. 2014 400:S190-S193. |
Zelickson, Brian D. et al., “Histological and Ultrastructural Evaluation of the Effects of a Radiofrequency-Based Nonablative Dermal Remodeling Device, A Pilot Study” Arch Dermatol, vol. 140, (Feb. 2004). |
Ulthera, Inc., Petition for Inter Partes Review filed Jul. 19, 2016 in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 63 pages (Filed Jul. 19, 2016). |
Ulthera Exhibit 1001, U.S. Pat. No. 6,113,559 to Klopotek, filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1002, Patent file history of U.S. Pat. No. 6,113,559 Klopotek filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1003, Declaration of Expert Witness Mark E. Schafer, Ph.D. filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1004, Curriculum Vitae of Mark E. Schafer, Ph.D. filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1005, International PCT Publication WO96/34568 Knowlton filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1006, French Patent No. 2,672,486, Technomed patent filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1007, English translation of French Patent No. 2,672,486, Technomed filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1008, International PCT Publication WO93/12742, Technomed PCT filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1009, English translation of International PCT Publication WO93/12742, Technomed PCT filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1010, U.S. Pat. No. 5,601,526, which claims priority to Technomed PCT filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1011, Patent file history for European Patent Application No. 98964890.2, Klopotek filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1012, Translator Declaration filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1013, U.S. Pat. No. 5,230,334 to Klopotek filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1014, U.S. Pat. No. 5,755,753 to Knowlton filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1015, Excerpts from The American Medical Association Encyclopedia of Medicine (1989) filed Jul. 19, 2016 in re IPR2016-01459. |
Ulthera Exhibit 1016, The Simultaneous Study of Light Emissions and Shock Waves Produced by Cavitation Bubbles, G. Gimenez, J. Acoust. Soc. Am. 71(4), Apr. 1982, pp. 839-847 (filed Jul. 19, 2016 in re IPR2016-01459). |
ULTHERA Exhibit 1017, Excerpts from Gray's Anatomy (1995) (filed Jul. 19, 2016 in re IPR2016-01459). |
Ulthera Exhibit 1018, Anatomy of the Superficial Venous System, Comjen G.M., Dermatol. Surg., 1995; 21:35-45 (filed Jul. 19, 2016 in re IPR2016-01459). |
Ulthera Exhibit 1019, Section 2.6 from Ultrasonics Theory and Application, by G.L. Gooberman (Hart Publishing Co., 1969) (filed Jul. 19, 2016 in re IPR2016-01459). |
Ulthera Exhibit 1020, Deep Local Hyperthermia for Cancer Therapy: ExternalElectromagnetic and Ultrasound Techniques, A.Y. Cheung and A. Neyzari, Cancer Research (Suppl.), vol. 44, pp. 4736-4744 (1984) (filed Jul. 19, 2016 in re IPR2016-01459). |
Decision on Institution of Inter Partes Review in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 20 pages [011] (Dated Jan. 23, 2017). |
Dermafocus Response to Institution of Inter Partes Review in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 73 pages [018] (Dated Apr. 26, 2017). |
Dermafocus Exhibit List in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 5 pages [019] (Dated Apr. 26, 2017). |
Dermafocus Exhibit 2002, Declaration of Mark Palmeri, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 136 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2003, Deposition of Dr. Mark Schafer, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 327 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2004, Amendment No. 4 to Ulthera Form S-1, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 308 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2005, Excerpt from Churchill Livingstone, Gray's Anatomy (38th ed. 1995), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 7 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2006, Bo Eklof et al., “Revision of the CEAP Classification forChronic Venous Disorders: Consensus Statement,” Acta Fac Med Naiss, vol. 25, No. 1 (2008), 3-10 in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 7 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2007, WebMD, “Varicose Veins and Spider Veins” downloaded from http://www.webmd.com/skin-problems-andtreatments/guide/varicose-spider-veins#1 in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 3 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2008, John M. Porter et al., “Reporting Standards in Venous Disease: An Update,” Journal of Vascular Surgery, vol. 21, No. 4 (1995), 635-645 in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 11 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2009, Kullervo Hynynen, “Review of Ultrasound Therapy,” 1997 Ultrasonics Symposium (1997), 1305-1313, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 9 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2010, A.G. Visioli et al., “Preliminary Results of a Phase I Dose Escalation Clinical Trial Using Focused Ultrasound in the Treatment of Localised Tumours,” European Journal of Ultrasound, vol. 9 (1999), 11-18, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 8 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2011, U.S. Pat. No. 5,143,063, issued on Sep. 1, 1992, Fellner, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 6 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2012, Hugh G. Beebe et al., “Consensus Statement: Classification and Grading of Chronic Venous Disease in the Lower Limbs,” European Journal of Vascular and Endovascular Surgery, vol. 12 (1996), 487-492, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 6 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2013, Excerpt from Mosby's Medical Dictionary (3rd ed. 1990), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 4 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2014, Excerpt from Miller-Keane Encyclopedia & Dictionary ofMedicine, Nursing, & Allied Health (5th ed. 1992), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 6 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2015, David J. Tibbs et al., Varicose Veins, Venous Disorders, and Lymphatic Problems in the Lower Limbs (1997), Chapter 4: Clinical Patterns of Venous Disorder I, 47-67, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 24 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2016, Mitchel P. Goldman et al., Varicose Veins and Telangiectasias (2nd ed. 1999), Chapter 22: Treatment of Leg Telangiectasias with Laser and High-Intensity Pulsed Light, 470-497, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 31 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2017, Email from Anderson to Klopotek dated May 25, 2004, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 1 page (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2018, List of Klopotek Patents, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 411 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2019, Declaration of Peter Klopotek Civil Action 15-cv-654-SLR,dated Nov. 2, 2016, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 1 page (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2020, “Our Technology,” downloaded fromhttp://jobs.ulthera.com/about on Apr. 10, 2017, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 4 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2021, C. Damianou and K. Hynynen, “Focal Spacing and Near-Field Heating During Pulsed High Temperature Ultrasound Therapy,” Ultrasound in Medicine & Biology, vol. 19, No. 9 (1993), 777-787, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 11 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2022, Excerpt from Mosby's Medical Dictionary (5th ed. 1997), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 5 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2023, Excerpt from Miller-Keane Encyclopedia & Dictionary of Medicine, Nursing, & Allied Health (6th ed. 1997), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 7 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2024, Excerpt from Stedman's Concise Medical Dictionary (3 rd ed. 1997), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 4 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2025, Excerpt from Taber's Cyclopedic Medical Dictionary (18th ed. 1997), in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 9 pages (Filed Apr. 26, 2017). |
Dermafocus Exhibit 2026, Bo Eklof et al., “Revision of the CEAP Classification for Chronic Venous Disorders: Consensus Statement,” Journal of Vascular Surgery, vol. 40, No. 6 (2004), 1248-1252.el, in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 6 pages (Filed Apr. 26, 2017). |
Ulthera, Inc., Reply in Support of Petition for Inter Partes Review in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 33 pages (Filed Aug. 2, 2017). |
Ulthera Exhibit 1022, Use of the Argon and Carbon Dioxide Lasers for Treatment ofSuperficial Venous Varicosities of the Lower Extremity, D. Apfelberg et al., Lasers in Surgery and Medicine, vol. 4.3, pp. 221-231 (1984) (filed Aug. 2, 2017 in re IPR2016-01459). |
Ulthera Exhibit 1023, 532-Nanometer Green Laser Beam Treatment of SuperficialVaricosities of the Lower Extremities, T. Smith et al., Lasers in Surgery and Medicine, vol. 8.2, pp. 130-134 (1988) (filed Aug. 2, 2017 in re IPR2016-01459). |
Ulthera Exhibit 1024, Deposition Transcript of Dr. Mark Palmeri on Jul. 11, 2017 (filed Aug. 2, 2017 in re IPR2016-01459). |
Ulthera Exhibit 1025, Ulthera Oral Proceeding Demonstrative Slides (filed Oct. 2, 2017 in re IPR2016-01459). |
Dermafocus Exhibit 2027, DermaFocus Oral Proceeding Demonstrative Slides (filed Oct. 2, 2017 in re IPR2016-01459). |
PTAB Record of Oral Hearing held Oct. 4, 2017 in U.S. Pat. No. 6,113,559; IPR2016-01459; 67 pages (PTAB Document sent to Ulthera on Nov. 1, 2017). |
Final Written Decision of Inter Partes Review in Re U.S. Pat. No. 6,113,559; IPR2016-01459; 37 pages [030] (Entered Jan. 19, 2018). |
Ulthera, Inc., Petitioner Notice of Appeal to Federal Circuit 2018-1542 re: IPR2016-01459; 4 pages from [001] (no appendices) (Filed Feb. 9, 2018). |
Federal Circuit Order Granting Ulthera Motion to Remand, re: 2018-1542; 4 pages [022] (Dated May 25, 2018). |
Ulthera Brief (Corrected), Fed. Cir. Appeal Case 19-1006 from re: IPR2016-01459; 136 pages [030] (Dated Apr. 3, 2019). |
DermaFocus Brief (Corrected), Fed. Cir. Appeal Case 19-1006 from re: IPR2016-01459; 73 pages [032] (Dated Apr. 4, 2019). |
Pavicic et al., Microfocused ultrasound with visualization: Consensus on safety and review of energy-based devices, J Cosmet Dermatol Feb. 2022, vol. 21, Issue 2: pp. 636-647, published online Dec. 24, 2021. |
Number | Date | Country | |
---|---|---|---|
20230338005 A1 | Oct 2023 | US |
Number | Date | Country | |
---|---|---|---|
61059477 | Jun 2008 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 17410780 | Aug 2021 | US |
Child | 18214851 | US | |
Parent | 16703019 | Dec 2019 | US |
Child | 17410780 | US | |
Parent | 12996616 | US | |
Child | 16703019 | US |