Patent Grant
10354556
This application relates to surgical training tools, and in particular, to simulated tissue structures and organ models for teaching and practicing surgical procedures and methods for making them.
A highly-skilled operation technique is required of surgeons, in general, and, in particular, for performing laparoscopic surgical procedures. In laparoscopic surgery, several small incisions are made in the abdomen for the insertion of trocars or small cylindrical tubes approximately 5 to 10 millimeters in diameter through which surgical instruments and a laparoscope are placed into the abdominal cavity. The laparoscope illuminates the surgical field and sends a magnified image from inside the body to a video monitor giving the surgeon a close-up view of organs and tissues. The surgeon performs the operation by manipulating the surgical instruments placed through the trocars while watching the live video feed on a monitor. Because the surgeon does not observe the organs and tissues directly with the naked eye, visual information is obtained by a two-dimensional image on a monitor instead of a three-dimensional observation. The loss of information when presenting a three-dimensional environment via a two-dimensional image is substantial. In particular, depth perception is reduced when viewing a two-dimensional image as a guide for manipulating instruments in three dimensions.
Furthermore, because the trocars are inserted through small incisions and rest against the abdominal wall, the manipulation of instruments is restricted by the abdominal wall which has a fulcrum effect on the instrument. The fulcrum effect defines a point of angulation that constrains the instrument to limited motion. Also, hand motion in one linear direction causes magnified tip motion in the opposite direction. Not only is the instrument motion viewed on the screen in the opposite direction, but also, the magnified tip motion is dependent on the fraction of the instrument length above the abdominal wall. This lever effect not only magnifies motion but also magnifies tool tip forces that are reflected to the user. Hence, the operation of an instrument with a fulcrum requires intentional learning and practice and is not intuitively obvious.
Also, surgical instruments are placed through ports having seals which induce a stick-slip friction caused by the reversal of tool directions. For example, stick-slip friction may arise from the reversal of tool directions when, for example, quickly changing from pulling to pushing on tissue. During such motion, rubber parts of the seals rub against the tool shaft causing friction or movement of the seal with the seal before the friction is overcome and the instrument slides relative to the seal. Stick-slip friction, or oil-canning, at the seal and instrument interface creates a non-linear force.
Hand-eye coordination skills are necessary and must be practiced in order to correlate hand motion with tool tip motion especially via observation on a video monitor. Also, in laparoscopic surgery, tactile sensation through the tool is diminished. Because haptics are reduced or distorted, the surgeon must develop a set of core haptic skills that underlie proficient laparoscopic surgery. The acquisition of all of these skills is one of the main challenges in laparoscopic training and the present invention is aimed at improving systems and methods for laparoscopic skills training and technique performance.
Not only do new practitioners have to learn laparoscopic skills, but also, experienced laparoscopic surgeons seek to polish old skills as well as to learn and practice new surgical techniques that are unique to newly introduced surgical procedures. While training can be acquired in the operating room, interest in devising faster and more efficient training methods, preferably outside the operating room has increased. Surgeons that attain a reasonable level of skills outside the operating room are better prepared when they enter the operating room and, thereby, valuable operating room experience can thus be optimized, lowering the risk to patients and reducing costs. To acquaint surgeons with basic surgical skills outside the operating room, various simulators have been devised and tested. An example of a surgical simulator is the SIMSEI® laparoscopic trainer manufactured by Applied Medical Resources Corporation in California and described in U.S. Pat. No. 8,764,452 incorporated by reference herein in its entirety. The SIMSEI® laparoscopic trainer employs three-dimensional live or fake organs inside a simulated abdominal cavity that is obscured from direct observation by the user.
Use of a live human or animal organ in a laparoscopic simulator requires freshness for the internal organ. Also, live organs require sanitary arrangements to be made to protect the trainee from being infected by germs and the like. Additional costs are also required for the sanitary management and sterilization of instruments which are used after the exercise of a surgical operation is performed. Also, the used live organ must be properly disposed. Furthermore, the smell of a live organ can be fowl and may distract the trainee from focusing on techniques and skills. Therefore, artificial organs and tissues that simulate live organs and tissues are desirable so that live organs can be replaced in surgical training.
Many artificial organs have been used in place of live human or animal organs in surgical training. Typically, these artificial organ models are made of silicone, urethane elastomer, styrene elastomer or the like. These artificial organs must respond properly when incised, manipulated or sutured, for example, and provide the same feeling and tactile characteristics as in real life surgery. However, many artificial organs lack certain properties and realism that are necessary to bridge the gap between artificial and real organs. Furthermore, the degree of realism must be targeting to provide means for teaching the skills that are peculiar to laparoscopic skills training. As such, certain realisms may be more important in a laparoscopic environment when compared to an open surgical environment. Therefore, there is a need for artificial organs and tissues and, in particular, for artificial organs and tissues that are targeted for laparoscopic skills training. The present invention sets forth new artificial organs and tissues that are realistic and targeted for laparoscopic skills training. The present invention also provides the methods of manufacturing such artificial organs and tissues.
According to one aspect of the invention, a simulated tissue structure and method of manufacturing it are provided. The simulated tissue structure includes a combination of two materials that are attached together wherein one of the materials forms a hollow anatomical structure configured to contain the other material. The two materials are attached in an anatomically advantageous manner such that the inner surface of the outer material closely conforms to the outer surface of the other. Also, the internal material has a different and more rigid characteristic relative to the external material and the anatomical geometry formed by the outer material would normally make insertion of the internal material into the external geometry damaging to the outer geometry, difficult to accomplish and would reduce the realism arising from compensations, such as repairing and gluing, necessary due to damaging insertion. The method of manufacture of the present invention includes the step of applying a first material in an uncured state directly onto the second material in a solid state to encase or encompass in whole or in part the second material; the second material defines the size and shape of at least part of the first material and forms a unitary and connected construction with the first material that is also easy to remove from a mandrel.
According to another aspect of the invention, a method of making a simulated tissue structure is provided. The method includes the step of providing a mandrel having a proximal end, a distal end and a longitudinal axis wherein the distal end of the mandrel includes an interlocking portion having a length. The method includes the step of providing an inner portion of a simulated tissue structure. The inner portion has a lumen sized and configured to receive the interlocking portion such that the entire length of the interlocking portion is located inside the lumen. The method includes the step of placing the inner portion onto the mandrel. The method further includes the step of placing the interlocking portion of the mandrel into the lumen of the inner portion. The method includes the steps of rotating the mandrel about the longitudinal axis, applying uncured silicone onto the inner portion, curing the silicone to form an outer portion that surrounds the inner portion, and removing the inner portion and the outer portion as one unit from the mandrel.
According to another aspect of the invention, a method of making a simulated tissue structure is provided. The method includes the step of providing a simulated anatomical structure. The method includes the step of providing a mandrel having a longitudinal axis, a proximal end and a distal end. The mandrel is configured to removably attach to the simulated anatomical structure. The method includes the step of connecting the simulated anatomical structure to the mandrel at a location along the longitudinal axis. The method includes the step of rotating the mandrel and connected simulated anatomical structure. The method includes the step of applying a second material in an uncured state to the mandrel and to the simulated anatomical structure. The method includes the step of allowing the second material to cure onto the simulated anatomical structure and mandrel to form a simulated tissue structure in which the simulated anatomical structure is surrounded in a thin shell of the second material. The simulated tissue structure has at least one lumen defined by the second material cured onto the mandrel. The method includes the steps of attaching the second material to the simulated anatomical structure, and removing the simulated anatomical structure with the attached second material.
According to another aspect of the invention, a simulated tissue structure is provided. The simulated anatomical structure has a proximal end and a distal end of a first material located inside a thin shell of a second material having a proximal end and a distal end. The simulated anatomical structure is attached to the second material. The simulated anatomical structure has a first diameter and a first lumen at the proximal end and the second material has a second lumen having a second diameter at the proximal end wherein the first lumen is substantially aligned with the second lumen.
According to another aspect of the invention, a method of making a simulated tissue structure is provided. The method includes the step of providing a planar first base layer. The method includes the step of providing a first stencil having at least one hole, and applying the first stencil onto the first base layer. The method includes the step of applying a first stencil layer onto the first base layer via the first stencil. The method includes the steps of removing the first stencil, providing a planar second base layer, and applying a second base layer over the stencil layer and first base layer. The method further includes the step of adhering the second base layer to the first base layer.
According to another aspect of the invention, a simulated tissue structure is provided. The simulated tissue structure includes a planar first base layer having a first side and a second side defining a substantially uniform thickness therebetween. The simulated tissue structure includes a planar second base layer having a first side and a second side defining a substantially uniform thickness therebetween. The second side of the second base layer faces the first side of the first base layer. The second base layer is adhered to the first base layer. The simulated tissue structure further includes at least one functional layer comprising a functional material located between the first base layer and the second base layer wherein the functional layer is formed via a stencil having at least one hole for applying the functional material.
Turning now to
The simulated tissue structure 10 further includes an inner portion 18 that is located inside the cavity 14 of the outer portion 12. The inner portion 18 includes an outer surface and an inner surface. The inner surface of the outer portion 12 closely conforms to the outer surface of the inner portion 18. The foam inner portion 18 is connected to the outer portion 12. In the variation shown in
Turning now to
Alternatively, and turning now to
The method of manufacturing the simulated tissue structure 10 will now be described. A mandrel 30 is used to manufacture the simulated anatomy. The mandrel 30 is typically connected to motor that rotates the mandrel 30 about its longitudinal axis. A mold, typically a mold having a desired shape such as a shape of an anatomical portion to be formed, is attached to the mandrel 30. When the motor is turned on, the mandrel 30 rotates and uncured silicone such as uncured PCRTVS is applied to the rotating mold that is connected to the mandrel 30. As the uncured silicone begins to cure, it assumes the shape of the underlying mold. Uncured silicone is applied such as by painting layers, spraying, or dipping the mold. When the application of silicone is completed, the uncured silicone is allowed to cure and then the resulting simulated tissue structure 10 is removed from mold and the mandrel 30 to create a hollow tissue structure of a desired shape. Typical hollow organs that can be created using this method include rectums, ovaries, fallopian tubes, vasculature, uteri and other organs.
Turning now to
Turning now to
As the mandrel 30 and attached inner portion 18 is rotated, uncured silicone such as PCRTVS is applied to cover at least the anatomical portion 38A and inner portion 18 and where applicable, a second anatomical portion 38B that is proximal to the interlocking portion 36 as shown in
Once the silicone cures, the outer portion 12 on the second anatomical portion 38B is rolled along the mandrel 30 towards the inner portion 18 or proximal end of the mandrel 30 and then the inner portion 18 and silicone outer portion 12 can be easily removed from the mandrel 30 as a single unit. The rolling of proximal end of the outer portion 12 helps to relieve any frictional forces between the outer portion 12 and the mandrel 30 to facilitate removal of the final anatomical model. As explained earlier, if the inner portion 18 is made of silicone foam then the uncured silicone will, as it cures, interlock, attach and connect with the silicone foam more strongly than if the inner portion 18 was made of urethane foam. This stronger bond will help in removing the silicone outer layer 12 and the attached inner portion 18 together more easily. Mold release or resist can be applied to the anatomical portion 38 and cylindrical portion of the mandrel 30 to facilitate removal of the outer portion 12 and inner portion 18 resulting in the simulated tissue structure 10 of
This method can be used to make fallopian tubes with ectopic pregnancies as just described above wherein the inner portion 18 simulates an ectopic pregnancy and the silicone outer portion 12 simulates the fallopian tube. The process can be used to make a wide range of other anatomies. The method adapted for making ovaries and ovaries with cysts with fallopian tubes will be described hereinbelow. Other anatomies that can be simulated include healthy and fibroid uteri. The foam of the inner portion 18 can be rigid or flexible and, as described above, it can be made of urethane, silicone or other material. Also, the simulated tissue could be any material other than silicone that can be applied to a mandrel by dipping, painting, spraying, etc.
Also, the method can be combined with a the steps of providing a mesh sleeve, for example, made of nylon mesh, placing the mesh sleeve onto the mandrel 30 and, applying the material of the outer portion 12 such as uncured silicone. The uncured silicone if applied to the mesh will pour over the mesh material and cure integrally into the mesh. Similarly, mesh applied to uncured silicone will cure integrally together. The mesh advantageously makes the outer portion 12 capable of holding sutures for the practice of suturing certain anatomies.
Turning now to
Turning now to
Turning now to
A simulated cyst, tumor or other anatomical variation is placed in the dimple 40 and attached thereto or held in place with adhesive or with the simultaneous application of wet silicone constituting the outer portion 18. As the mandrel 30 and attached inner portion 18 and attached cysts are rotated uncured silicone, such as PCRTVS, is applied to cover at least the inner portion 18 and attached cysts. As the mandrel 30 rotates, more uncured silicone is applied to achieve a desired thickness of material. The uncured silicone begins to cure and additional uncured silicone can be continuously applied. The uncured silicone is applied on the inner portion 18 and may also be applied on the mandrel 30. Uncured silicone may be applied with by painting with a brush, spraying, dipping or other manner. Rotation of the mandrel 30 prevents the silicone from curing to form unevenly covered areas. After the silicone is completely cured, the outer portion 12 is formed comprising the silicone layer about the mandrel 30. Hence, the outer surface of the inner portion 18 will define the size and shape of at least part of the inner surface of the outer portion 12. Once the silicone cures, a portion of it at the mandrel 30 may be rolled distally along the longitudinal axis. The inner portion 18 may be grasped and pulled distally to remove the construct from the mandrel 30. The foam inner portion 18 and silicone outer portion 12 can be easily removed from the mandrel 30 as a single unit. The resulting simulated tissue structure 10 as removed from the mandrel 30 is illustrated in
Turning now to
The present invention creates a simulated tissue structure 10 that advantageously combines silicone material with foam material that are attached in an anatomically advantageous manner to represent ectopic pregnancies, cysts, fibroids, tumors or other anatomical portion in combination with a hollow anatomical structure. The method includes applying silicone directly onto the inner portion to form the outer portion and simultaneously mold the outer portion to the inner portion in an integral fashion to form a unitary construction. Otherwise, the silicone outer portion would have to be formed separately on a mandrel and removed once cured. Then, the formed hollow silicone structure would have to be cut open and a foam piece would then be inserted into the silicone structure. Cutting open the silicone structure would be the only way to accommodate a size and shape of foam material while retaining the anatomical characteristics such as narrowed tubular structures on one or more ends of the foam inner portion. After the foam inner portion is inserted, the cut silicone would then have to be glued back together to complete the anatomy in question creating an inferior simulated tissue structure. By using the foam inner portion 18 as part of the forming mandrel 30 that is removable and integrated into the simulated tissue structure, the present invention advantageously eliminates several steps in the manufacturing process including cutting open a hollow silicone shape, inserting a foam inner piece into the opening created by the cutting, and then gluing the opening closed when finished. Cutting the hollow shape is necessitated by the size of the inner portion relative to the surrounding tubular anatomical structure. Forcing a foam insert in through an opening in the hollow silicone shape would result in the silicone tearing during the process. Hence, the present invention solves many problems to create an ideal simulated tissue structure. Furthermore, removal of silicone material from a mandrel 30 is complicated because the silicone is notoriously sticky and complex shapes such as fallopian tubes with ectopic pregnancy can be exceedingly difficult to remove from the mandrel without incurring damage to the work-piece. The addition of the foam insert to the mandrel greatly reduces the difficult of removing the silicone part from the mandrel because part of the silicone part is attached to the foam insert which easily slides off the mandrel instead of to the mandrel directly. Portions of silicone attached to an anatomical portion 30 or cylindrical portion of the mandrel 30 can be first bunched near the foam inner portion and then the inner portion 18 can easily slide off of the mandrel 30. As previously mentioned, the foam can represent a separate component entirely such as a cyst, fibroid or tumor or just serve as a filler material or tissue layer of different density to help certain anatomy to retain a three-dimensional shape or define and replicate certain anatomical characteristics. Additionally, having the silicone cure on the foam adds an element of difficulty to simulated training procedures which can be desirable in certain situations as dissection between tissue planes is not always easy. The present invention provides a simulated tissue structure with all of these advantages. Also, as mentioned previously, variants can include different material selection for the inner portion 18 including varying densities of foam and plastics can be used depending on the desired feel of the anatomical component.
The simulated tissue structure 10 of the present invention is particularly suited for laparoscopic procedures and may be employed with a laparoscopic trainer; however, the invention is not so limited and the simulated tissue structure 10 of the present invention can be used alone to practice various surgical procedures equally effectively.
Turning now to
One version of this process involves using a stencil to apply mold release or resist to silicone sheets in a desired pattern. By using stencils, screens, or lithographic plates, resist coverage can be tailored in a specific pattern such as dots, halftone or other pattern to give a specific area a percentage of adhesion or relative adhesion between two sheets of material. For example, if a stencil includes a pattern that is approximately 50% open and it is used to apply a stencil layer of resist material to a silicone layer of equal area, the adhesion of the adjacent silicone layer will be reduced by approximately 50%. The pattern of mold release/resist is applied to a first surface of a previously-cured sheet of silicone via the stencil, screen or other plate. This prepared sheet is then laid on top of an uncured sheet of silicone that may or may not be resident inside a mold. The combination of the cured silicone sheet with a stencil layer and the uncured silicone layer is then given time to cure. Upon curing, a sandwiched construct results having variable interface characteristics across the interface plane due to the stencil layer. This method, when repeated, with multiple layers builds up a specified thickness of simulated tissue with desired properties including variability of X-Y plane interface, properties along the Z-axis, in addition to and/or separate from material properties and visual characteristics. A higher percentage of area covered by dots of mold release/resist via the stencil, plate or screen will build up a tissue that feels softer and easier to pull apart. A lower percentage of area covered by mold release/resist dots via the stencil, plate or screen will build up a solid block that feels harder and is more monolithic and will be more difficult to cut or pull apart using surgical instruments.
In another variation, instead of applying resist or mold release via a stencil, plate or screen to a layer of cured silicone, silicone or other adhesive is applied via the stencil, plate, mask, or screen in a particular pattern or halftone to a layer of cured silicone which can then be used to join two previously cured silicone sheets creating two layers that are selectively adhered having variable adhesion along the interface plane and subsequently built up with additional layers to create a multiple layer construct having variable adhesion in the interfacing planes along the Z-axis. Hence, the stencil layer is a functional layer, the function of which may be selected from the group of adhesion, release, and color.
The pattern on the stencil, plate or screen is not limited to dots and material may be applied creating stencil layers for a simulated tissue structure where lines, webs, ovals, squares, curves or other shapes of various thicknesses and colors are created by the stencil layer, for example, to mimic vasculature, musculature, fatty layers or other complex organs and tissues in a two-dimensional layer and intercommunicating with adjacent layers in a three-dimensional construct in which structures transition and continue across multiple layers. This method is used to build an overall desired thickness of material of tissue structure to be used in surgical simulation.
In addition, each of these techniques, applying resist or adhesive using a stencil, screen or plate employing printmaking methods, can be used with textured sheets of silicone and casting dishes to further tailor the feel and response of the material. Also, color can be introduced to simulate different anatomical layers and constructs. The addition of color aids the user in navigation during surgical simulation as well as assessment after the simulation exercise is completed. For example, a surgeon practicing an incision will know that the incision through one or more base layers is too deep if a certain color such as red becomes visible wherein the red color is provided in a functional layer serving the function of a visual indicator for training purposes. Of course, color may be employed in at least the functional layer to provide various surgical markers, anatomy, and targets such as tumors and the like. Similarly, for example, after the simulation exercise is completed, an assessment of the layers can be made to ascertain the accuracy of a procedure for purposes of training and evaluation. For example, layers can be separated and examined to see if an incision penetrated too deeply or to see if care was taken to separate layers carefully without unnecessary cutting into unwanted anatomy.
In one variation, a block of simulated tissue is created using the resist method described above to create a block of simulated tissue comprising a plurality of layers where the layers gradually transition from flesh tone to white to red. When working with this multi-layered simulated tissue structure having a gradation of color and/or interface adhesion properties, dissection in the flesh tone and white layers would be positively regarding with respect to the simulation exercise. Also, positive regard would be attributed in the evaluation to respect for tissue techniques that illustrate the surgeon's skill to separate instead of cutting muscle fibers in the making of an incision through the abdomen for example. The variable adhesion characteristics of the simulated tissue model are used to facilitate the training of the separation of muscle fibers and other respect for tissue techniques. Colored layers can be used in the post-exercise assessment by examining the construct to see if cuts extend through the white layer(s) and into the red layer(s), for example. If the red layer(s), for example, have been cut, the surgeon and the assessor will know that they have gone too far and continued training is required. The present invention advantageously improves the feel and functionality of a simulated tissue structure especially in a training environment while providing live feedback to the surgeon and assessment means to the trainer especially in regard to dissection.
By creating stencils, screens, masks or plates such as silk screens or lithographic plates to be used to create simulated tissue for specific human or animal anatomy, specific, desirable properties can be achieved. By controlling the percent area and shape of adhesion or resist between two or more layers of silicone or KRATON or hydrogel, etc., a higher degree of realism can be achieved in surgical simulation and provide a way to train surgeons that was not previously possible.
Turning now to
The holes 122 shown in
Turning now to
The next step of the method of forming a simulated tissue structure according to the present invention is shown in
The next step of the method of forming the simulated tissue structure according to the present invention is shown in
Still referencing
Still referencing
Turning now to
Turning now to
The simulated tissue structure 110 formed according to the present invention advantageously introduces functional layers that are printed with a stencil between non-functional base or support layers. In the printing of functional layers, the stencil is used to pattern the material onto the base layers and then the stencil is removed. Each functional layer may serve one or more functional purpose. Also, multiple functional layers may be printed consecutively between two adjacent base layers or different functional layers may be printed at different interface locations. As described above, a stencil layer may serve the function of providing a mechanical interaction between the two base layers. For example, the location of adhesion and/or release as well as the degree of adhesion and/or release may be provided by a functional layer printed in a particular shape, pattern to provide a locus of mechanical interaction and the type of material printed whether release/adhesive or other material provides the type or strength of the mechanical property to create the customized property for that particular interface. Areas of weak mechanical connection can be provided by printing release/resist material or the like. Areas of strong mechanical attachment between base layers can be provided by printing uncured silicone onto a base layer of cured silicone, or printing adhesive, glue and the like. Another purpose served by a functional layer is providing a pathway for electrical conductivity such as for creating a simulated tissue structure suitable for practicing electro-surgery. In such a case, a hydrogel would be printed onto a base layer via the stencil. A fluidic circuit of hydrogel may be patterned to interconnect the dots or other pattern of the functional layer and to further connect the functional layer to a ground or power source. Creating a circuit may be provided by printing a conductive material other than hydrogel that includes conductive filaments or the like to impart pathways for conductivity as well as providing non-conductive areas/pathways. Another functional purpose that the functional layer may provide is suturability. In such a case, the stencil is used to lay down silicone with mesh, fiber and the like to strengthen areas for holding sutures. Another function for the stencil layer may be dissection. For example, a polyfill material may be employed and applied via a stencil onto a dry or wet silicone base layer to embed the polyfill material between the base layers in specific locations and then an adjacent wet layer of silicone may applied to create a functional interface that is easy to dissect or separate by cutting through the polyfill fibers. The functional layer may serve to provide realistic coloring to a layer or when used in conjunction with transparent or semi-transparent base layers where the color patterns can overlap with other color functional layers to create an overall effect. Also, as described above a functional layer may be used to lay down anatomical structures between and/or across base layers. Unique shapes representative of various anatomical structures may be formed using a stencil including but not limited to for example printing the shape and color of Toldt's fascia, omentum, anatomical landmarks/structures and the like. In another variation of the present invention, the stencil is not removed from the construct but left in to become an integral piece of the simulated tissue structure. For example, the stencil may be shaped to represent an anatomical bony structure or cartilage and located between two base layers in which an adjacent base layer is applied while uncured so as to interlock with the adjacent base layer to embed the stencil. In another variation, the stencil does not represent an anatomical structure when left in but is designed and configured to impart structural rigidity to the resulting structure. In yet another variation, the stencil is not employed to apply an intermediate functional layer between two base layers, but instead, serves to merely permit the application of an adjacent uncured silicone base layer through the holes of the stencil for attachment to the adjacent base layer in select areas defined by the stencil openings.
The simulated tissue structure 110 of the present invention is particularly suited for laparoscopic procedures and may be employed with a laparoscopic trainer; however, the invention is not so limited and the simulated tissue structure 110 of the present invention can be used alone to practice first entry surgical procedures equally effectively.
It is understood that various modifications may be made to the embodiments of the artificial tissue simulations and methods of making them disclosed herein. Therefore, the above description should not be construed as limiting, but merely as exemplifications of preferred embodiments. Those skilled in the art will envision other modifications within the scope and spirit of the present disclosure.
This application is a continuation of International Application No. PCT/US2016/018697 entitled “Simulated tissue structures and methods” filed on Feb. 19, 2016 which claims priority to and benefit of U.S. Provisional Patent Application No. 62/118,179 entitled “Method of making simulated tissue using stencils” filed on Feb. 19, 2015 and U.S. Provisional Patent Application No. 62/119,542 entitled “Foam-on-mandrel method of making simulated anatomy” filed on Feb. 23, 2015 all of which are incorporated herein by reference in their entireties.
| Number | Name | Date | Kind |
|---|---|---|---|
| 184573 | Becker | Nov 1876 | A |
| 2127774 | Jacobs | Aug 1938 | A |
| 2284888 | Arneil, Jr. | Jun 1942 | A |
| 2324702 | Hoffman et al. | Jul 1943 | A |
| 2345489 | Lord | Mar 1944 | A |
| 2495568 | Coel | Jan 1950 | A |
| 3766666 | Stroop | Oct 1973 | A |
| 3775865 | Rowan | Dec 1973 | A |
| 3789518 | Chase | Feb 1974 | A |
| 3921311 | Beasley et al. | Nov 1975 | A |
| 3991490 | Markman | Nov 1976 | A |
| 4001951 | Fasse | Jan 1977 | A |
| 4001952 | Kleppinger | Jan 1977 | A |
| 4321047 | Landis | Mar 1982 | A |
| 4323350 | Bowden, Jr. | Apr 1982 | A |
| 4332569 | Burbank | Jun 1982 | A |
| 4371345 | Palmer et al. | Feb 1983 | A |
| 4386917 | Forrest | Jun 1983 | A |
| 4459113 | Boscaro Gatti et al. | Jul 1984 | A |
| 4481001 | Graham et al. | Nov 1984 | A |
| 4596528 | Lewis et al. | Jun 1986 | A |
| 4726772 | Amplatz | Feb 1988 | A |
| 4737109 | Abramson | Apr 1988 | A |
| 4789340 | Zikria | Dec 1988 | A |
| 4832978 | Lesser | May 1989 | A |
| 4867686 | Goldstein | Sep 1989 | A |
| 4907973 | Hon | Mar 1990 | A |
| 4938696 | Foster et al. | Jul 1990 | A |
| 4940412 | Blumenthal | Jul 1990 | A |
| 5061187 | Jerath | Oct 1991 | A |
| 5083962 | Pracas | Jan 1992 | A |
| 5104328 | Lounsbury | Apr 1992 | A |
| 5149270 | McKeown | Sep 1992 | A |
| 5180308 | Garito et al. | Jan 1993 | A |
| 5230630 | Burgett | Jul 1993 | A |
| 5273435 | Jacobson | Dec 1993 | A |
| 5295694 | Levin | Mar 1994 | A |
| 5310348 | Miller | May 1994 | A |
| 5318448 | Garito et al. | Jun 1994 | A |
| 5320537 | Watson | Jun 1994 | A |
| 5358408 | Medina | Oct 1994 | A |
| 5368487 | Medina | Nov 1994 | A |
| 5380207 | Siepser | Jan 1995 | A |
| 5403191 | Tuason | Apr 1995 | A |
| 5425644 | Szinicz | Jun 1995 | A |
| 5425731 | Daniel et al. | Jun 1995 | A |
| 5472345 | Eggert | Dec 1995 | A |
| 5518406 | Waters | May 1996 | A |
| 5518407 | Greenfield et al. | May 1996 | A |
| 5520633 | Costin | May 1996 | A |
| 5541304 | Thompson | Jul 1996 | A |
| 5620326 | Younker | Apr 1997 | A |
| 5720742 | Zacharias | Feb 1998 | A |
| 5722836 | Younker | Mar 1998 | A |
| 5727948 | Jordan | Mar 1998 | A |
| 5743730 | Clester et al. | Apr 1998 | A |
| 5762458 | Wang et al. | Jun 1998 | A |
| 5769640 | Jacobus et al. | Jun 1998 | A |
| 5775916 | Cooper et al. | Jul 1998 | A |
| 5785531 | Leung | Jul 1998 | A |
| 5800178 | Gillio | Sep 1998 | A |
| 5803746 | Barrie et al. | Sep 1998 | A |
| 5807378 | Jensen et al. | Sep 1998 | A |
| 5810880 | Jensen et al. | Sep 1998 | A |
| 5814038 | Jensen et al. | Sep 1998 | A |
| 5850033 | Mirzeabasov et al. | Dec 1998 | A |
| 5855583 | Wang et al. | Jan 1999 | A |
| 5873732 | Hasson | Feb 1999 | A |
| 5873863 | Komlosi | Feb 1999 | A |
| 5908302 | Goldfarb | Jun 1999 | A |
| 5947743 | Hasson | Sep 1999 | A |
| 5951301 | Younker | Sep 1999 | A |
| 6080181 | Jensen et al. | Jun 2000 | A |
| 6083008 | Yamada et al. | Jul 2000 | A |
| 6113395 | Hon | Sep 2000 | A |
| 6234804 | Yong | May 2001 | B1 |
| 6271278 | Park et al. | Aug 2001 | B1 |
| 6336812 | Cooper et al. | Jan 2002 | B1 |
| 6398557 | Hoballah | Jun 2002 | B1 |
| 6413264 | Jensen et al. | Jul 2002 | B1 |
| 6474993 | Grund et al. | Nov 2002 | B1 |
| 6485308 | Goldstein | Nov 2002 | B1 |
| 6488507 | Stoloff et al. | Dec 2002 | B1 |
| 6497902 | Ma | Dec 2002 | B1 |
| 6511325 | Lalka et al. | Jan 2003 | B1 |
| 6517354 | Levy | Feb 2003 | B1 |
| 6568941 | Goldstein | May 2003 | B1 |
| 6589057 | Keenan et al. | Jul 2003 | B1 |
| 6620174 | Jensen et al. | Sep 2003 | B2 |
| 6654000 | Rosenberg | Nov 2003 | B2 |
| 6659776 | Aumann et al. | Dec 2003 | B1 |
| 6773263 | Nicholls et al. | Aug 2004 | B2 |
| 6780016 | Toly | Aug 2004 | B1 |
| 6817973 | Merril et al. | Nov 2004 | B2 |
| 6820025 | Bachmann et al. | Nov 2004 | B2 |
| 6854976 | Suhr | Feb 2005 | B1 |
| 6857878 | Chosack et al. | Feb 2005 | B1 |
| 6863536 | Fisher et al. | Mar 2005 | B1 |
| 6866514 | Von Roeschlaub et al. | Mar 2005 | B2 |
| 6887082 | Shun | May 2005 | B2 |
| 6929481 | Alexander et al. | Aug 2005 | B1 |
| 6939138 | Chosack et al. | Sep 2005 | B2 |
| 6950025 | Nguyen | Sep 2005 | B1 |
| 6960617 | Omidian et al. | Nov 2005 | B2 |
| 6997719 | Wellman et al. | Feb 2006 | B2 |
| 7008232 | Brassel | Mar 2006 | B2 |
| 7018327 | Conti | Mar 2006 | B1 |
| 7025064 | Wang et al. | Apr 2006 | B2 |
| 7056123 | Gregorio et al. | Jun 2006 | B2 |
| 7080984 | Cohen | Jul 2006 | B1 |
| 7118582 | Wang et al. | Oct 2006 | B1 |
| 7255565 | Keegan | Aug 2007 | B2 |
| 7269532 | David et al. | Sep 2007 | B2 |
| 7272766 | Sakezles | Sep 2007 | B2 |
| 7300450 | Vleugels et al. | Nov 2007 | B2 |
| 7364582 | Lee | Apr 2008 | B2 |
| 7404716 | Gregorio et al. | Jul 2008 | B2 |
| 7419376 | Sarvazyan et al. | Sep 2008 | B2 |
| 7427199 | Sakezles | Sep 2008 | B2 |
| 7431189 | Shelton, IV et al. | Oct 2008 | B2 |
| 7441684 | Shelton, IV et al. | Oct 2008 | B2 |
| 7465168 | Allen et al. | Dec 2008 | B2 |
| 7467075 | Humphries et al. | Dec 2008 | B2 |
| 7544062 | Hauschild et al. | Jun 2009 | B1 |
| 7549866 | Cohen et al. | Jun 2009 | B2 |
| 7553159 | Arnal et al. | Jun 2009 | B1 |
| 7575434 | Palakodeti | Aug 2009 | B2 |
| 7594815 | Toly | Sep 2009 | B2 |
| 7621749 | Munday | Nov 2009 | B2 |
| 7646901 | Murphy et al. | Jan 2010 | B2 |
| 7648367 | Makower et al. | Jan 2010 | B1 |
| 7648513 | Green et al. | Jan 2010 | B2 |
| 7651332 | Dupuis et al. | Jan 2010 | B2 |
| 7677897 | Sakezles | Mar 2010 | B2 |
| 7775916 | Mahoney | Aug 2010 | B1 |
| 7780451 | Willobee et al. | Aug 2010 | B2 |
| 7802990 | Korndorffer et al. | Sep 2010 | B2 |
| 7803151 | Whitman | Sep 2010 | B2 |
| 7806696 | Alexander et al. | Oct 2010 | B2 |
| 7819799 | Merril et al. | Oct 2010 | B2 |
| 7833018 | Alexander et al. | Nov 2010 | B2 |
| 7837473 | Koh | Nov 2010 | B2 |
| 7850454 | Toly | Dec 2010 | B2 |
| 7850456 | Chosack et al. | Dec 2010 | B2 |
| 7854612 | Frassica et al. | Dec 2010 | B2 |
| 7857626 | Toly | Dec 2010 | B2 |
| 7866983 | Hemphill et al. | Jan 2011 | B2 |
| 7931470 | Alexander et al. | Apr 2011 | B2 |
| 7931471 | Senagore et al. | Apr 2011 | B2 |
| 7988992 | Omidian et al. | Aug 2011 | B2 |
| 7993140 | Sakezles | Aug 2011 | B2 |
| 7997903 | Hasson et al. | Aug 2011 | B2 |
| 8007281 | Toly | Aug 2011 | B2 |
| 8007282 | Gregorio et al. | Aug 2011 | B2 |
| 8016818 | Ellis et al. | Sep 2011 | B2 |
| 8017107 | Thomas et al. | Sep 2011 | B2 |
| 8021162 | Sui | Sep 2011 | B2 |
| 8048088 | Green et al. | Nov 2011 | B2 |
| 8083691 | Goldenberg et al. | Dec 2011 | B2 |
| 8116847 | Gattani et al. | Feb 2012 | B2 |
| 8137110 | Sakezles | Mar 2012 | B2 |
| 8157145 | Shelton, IV et al. | Apr 2012 | B2 |
| 8197464 | Krever et al. | Jun 2012 | B2 |
| 8205779 | Ma et al. | Jun 2012 | B2 |
| 8221129 | Parry et al. | Jul 2012 | B2 |
| 8297982 | Park et al. | Oct 2012 | B2 |
| 8308817 | Egilsson et al. | Nov 2012 | B2 |
| 8323028 | Matanhelia | Dec 2012 | B2 |
| 8323029 | Toly | Dec 2012 | B2 |
| 8328560 | Niblock et al. | Dec 2012 | B2 |
| 8342851 | Speeg et al. | Jan 2013 | B1 |
| 8403674 | Feygin et al. | Mar 2013 | B2 |
| 8403675 | Stoianovici et al. | Mar 2013 | B2 |
| 8403676 | Frassica et al. | Mar 2013 | B2 |
| 8408920 | Speller | Apr 2013 | B2 |
| 8425234 | Sakezles | Apr 2013 | B2 |
| 8439687 | Morriss et al. | May 2013 | B1 |
| 8442621 | Gorek et al. | May 2013 | B2 |
| 8454368 | Ault et al. | Jun 2013 | B2 |
| 8459094 | Yanni | Jun 2013 | B2 |
| 8459520 | Giordano et al. | Jun 2013 | B2 |
| 8460002 | Wang et al. | Jun 2013 | B2 |
| 8465771 | Wan et al. | Jun 2013 | B2 |
| 8469715 | Ambrozio | Jun 2013 | B2 |
| 8469716 | Fedotov et al. | Jun 2013 | B2 |
| 8480407 | Campbell et al. | Jul 2013 | B2 |
| 8480408 | Ishii et al. | Jul 2013 | B2 |
| 8491309 | Parry et al. | Jul 2013 | B2 |
| 8500753 | Green et al. | Aug 2013 | B2 |
| 8512044 | Sakezles | Aug 2013 | B2 |
| 8517243 | Giordano et al. | Aug 2013 | B2 |
| 8521252 | Diez | Aug 2013 | B2 |
| 8535062 | Nguyen | Sep 2013 | B2 |
| 8544711 | Ma et al. | Oct 2013 | B2 |
| 8556635 | Toly | Oct 2013 | B2 |
| 8608483 | Trotta et al. | Dec 2013 | B2 |
| 8613621 | Hendrickson et al. | Dec 2013 | B2 |
| 8636520 | Iwasaki et al. | Jan 2014 | B2 |
| D699297 | Bahsoun et al. | Feb 2014 | S |
| 8641423 | Gumkowski | Feb 2014 | B2 |
| 8647125 | Johns et al. | Feb 2014 | B2 |
| 8678831 | Trotta et al. | Mar 2014 | B2 |
| 8679279 | Thompson et al. | Mar 2014 | B2 |
| 8696363 | Gray et al. | Apr 2014 | B2 |
| 8708213 | Shelton, IV et al. | Apr 2014 | B2 |
| 8708707 | Hendrickson et al. | Apr 2014 | B2 |
| 8764449 | Rios et al. | Jul 2014 | B2 |
| 8764452 | Pravong et al. | Jul 2014 | B2 |
| 8800839 | Beetel | Aug 2014 | B2 |
| 8801437 | Mousques | Aug 2014 | B2 |
| 8801438 | Sakezles | Aug 2014 | B2 |
| 8807414 | Ross et al. | Aug 2014 | B2 |
| 8808004 | Misawa et al. | Aug 2014 | B2 |
| 8808311 | Heinrich et al. | Aug 2014 | B2 |
| 8814573 | Nguyen | Aug 2014 | B2 |
| 8827988 | Belson et al. | Sep 2014 | B2 |
| 8840628 | Green et al. | Sep 2014 | B2 |
| 8870576 | Millon et al. | Oct 2014 | B2 |
| 8888498 | Bisaillon et al. | Nov 2014 | B2 |
| 8893946 | Boudreaux et al. | Nov 2014 | B2 |
| 8911238 | Forsythe | Dec 2014 | B2 |
| 8915742 | Hendrickson et al. | Dec 2014 | B2 |
| 8945095 | Blumenkranz et al. | Feb 2015 | B2 |
| 8961190 | Hart et al. | Feb 2015 | B2 |
| 8966954 | Ni et al. | Mar 2015 | B2 |
| 8968003 | Hendrickson et al. | Mar 2015 | B2 |
| 9008989 | Wilson et al. | Apr 2015 | B2 |
| 9017080 | Placik | Apr 2015 | B1 |
| 9026247 | White | May 2015 | B2 |
| 9050201 | Egilsson et al. | Jun 2015 | B2 |
| 9056126 | Hersel et al. | Jun 2015 | B2 |
| 9070306 | Rappel et al. | Jun 2015 | B2 |
| 9087458 | Shim et al. | Jul 2015 | B2 |
| 9096744 | Wan et al. | Aug 2015 | B2 |
| 9117377 | Shim et al. | Aug 2015 | B2 |
| 9119572 | Gorek et al. | Sep 2015 | B2 |
| 9123261 | Lowe | Sep 2015 | B2 |
| 9129054 | Nawana et al. | Sep 2015 | B2 |
| 9196176 | Hager et al. | Nov 2015 | B2 |
| 9226799 | Lightcap et al. | Jan 2016 | B2 |
| 9257055 | Endo et al. | Feb 2016 | B2 |
| 9265587 | Vancamberg et al. | Feb 2016 | B2 |
| 9295468 | Heinrich et al. | Mar 2016 | B2 |
| 9351714 | Ross et al. | May 2016 | B2 |
| 9336694 | Shim et al. | Jun 2016 | B2 |
| 9358682 | Ruiz Morales | Jun 2016 | B2 |
| 9364224 | Nicholas et al. | Jun 2016 | B2 |
| 9364279 | Houser et al. | Jun 2016 | B2 |
| 9370361 | Viola et al. | Jun 2016 | B2 |
| 9373270 | Miyazaki | Jun 2016 | B2 |
| 9387276 | Sun et al. | Jul 2016 | B2 |
| 9427496 | Sun et al. | Aug 2016 | B2 |
| 9439649 | Shelton, IV et al. | Sep 2016 | B2 |
| 9439733 | Ha et al. | Sep 2016 | B2 |
| 9449532 | Black et al. | Sep 2016 | B2 |
| 9468438 | Baber et al. | Oct 2016 | B2 |
| 20010019818 | Yong | Sep 2001 | A1 |
| 20020168619 | Provenza | Nov 2002 | A1 |
| 20030031993 | Pugh | Feb 2003 | A1 |
| 20030091967 | Chosack et al. | May 2003 | A1 |
| 20030176770 | Merril et al. | Sep 2003 | A1 |
| 20040005423 | Dalton et al. | Jan 2004 | A1 |
| 20040126746 | Toly | Jul 2004 | A1 |
| 20040248072 | Gray et al. | Dec 2004 | A1 |
| 20050008997 | Herman | Jan 2005 | A1 |
| 20050026125 | Toly | Feb 2005 | A1 |
| 20050084833 | Lacey et al. | Apr 2005 | A1 |
| 20050131390 | Heinrich et al. | Jun 2005 | A1 |
| 20050142525 | Cotin et al. | Jun 2005 | A1 |
| 20050192595 | Green et al. | Sep 2005 | A1 |
| 20050196739 | Moriyama | Sep 2005 | A1 |
| 20050196740 | Moriyama | Sep 2005 | A1 |
| 20050214727 | Stoianovici et al. | Sep 2005 | A1 |
| 20060046235 | Alexander et al. | Mar 2006 | A1 |
| 20060252019 | Burkitt et al. | Nov 2006 | A1 |
| 20060275741 | Chewning et al. | Dec 2006 | A1 |
| 20070074584 | Talarico et al. | Apr 2007 | A1 |
| 20070077544 | Lemperle et al. | Apr 2007 | A1 |
| 20070078484 | Talarico et al. | Apr 2007 | A1 |
| 20070148626 | Ikeda | Jun 2007 | A1 |
| 20070166682 | Yarin et al. | Jul 2007 | A1 |
| 20070197895 | Nycz et al. | Aug 2007 | A1 |
| 20070225734 | Bell et al. | Sep 2007 | A1 |
| 20070275359 | Rotnes et al. | Nov 2007 | A1 |
| 20080032272 | Palakodeti | Feb 2008 | A1 |
| 20080032273 | Macnamara et al. | Feb 2008 | A1 |
| 20080052034 | David et al. | Feb 2008 | A1 |
| 20080064017 | Grundmeyer, III et al. | Mar 2008 | A1 |
| 20080076101 | Hyde et al. | Mar 2008 | A1 |
| 20080097501 | Blier | Apr 2008 | A1 |
| 20080108869 | Sanders et al. | May 2008 | A1 |
| 20080187895 | Sakezles | Aug 2008 | A1 |
| 20080188948 | Flatt | Aug 2008 | A1 |
| 20080299529 | Schaller | Dec 2008 | A1 |
| 20080317818 | Griffith et al. | Dec 2008 | A1 |
| 20090068627 | Toly | Mar 2009 | A1 |
| 20090142739 | Wang et al. | Jun 2009 | A1 |
| 20090142741 | Ault et al. | Jun 2009 | A1 |
| 20090143642 | Takahashi et al. | Jun 2009 | A1 |
| 20090176196 | Niblock et al. | Jul 2009 | A1 |
| 20090187079 | Albrecht et al. | Jul 2009 | A1 |
| 20090246747 | Buckman, Jr. | Oct 2009 | A1 |
| 20090298034 | Parry et al. | Dec 2009 | A1 |
| 20090314550 | Layton | Dec 2009 | A1 |
| 20100047752 | Chan et al. | Feb 2010 | A1 |
| 20100094312 | Ruiz Morales et al. | Apr 2010 | A1 |
| 20100099067 | Agro | Apr 2010 | A1 |
| 20100167248 | Ryan | Jul 2010 | A1 |
| 20100167249 | Ryan | Jul 2010 | A1 |
| 20100167250 | Ryan et al. | Jul 2010 | A1 |
| 20100167253 | Ryan et al. | Jul 2010 | A1 |
| 20100167254 | Nguyen | Jul 2010 | A1 |
| 20100196867 | Geerligs et al. | Aug 2010 | A1 |
| 20100204713 | Ruiz Morales | Aug 2010 | A1 |
| 20100209899 | Park | Aug 2010 | A1 |
| 20100248200 | Ladak | Sep 2010 | A1 |
| 20100258611 | Smith et al. | Oct 2010 | A1 |
| 20100273136 | Kandasami et al. | Oct 2010 | A1 |
| 20100279263 | Duryea | Nov 2010 | A1 |
| 20100285094 | Gupta | Nov 2010 | A1 |
| 20100324541 | Whitman | Dec 2010 | A1 |
| 20110020779 | Hannaford et al. | Jan 2011 | A1 |
| 20110046637 | Patel et al. | Feb 2011 | A1 |
| 20110046659 | Ramstein et al. | Feb 2011 | A1 |
| 20110087238 | Wang et al. | Apr 2011 | A1 |
| 20110091855 | Miyazaki | Apr 2011 | A1 |
| 20110137337 | van den Dool et al. | Jun 2011 | A1 |
| 20110200976 | Hou et al. | Aug 2011 | A1 |
| 20110207104 | Trotta | Aug 2011 | A1 |
| 20110218550 | Ma | Sep 2011 | A1 |
| 20110244436 | Campo | Oct 2011 | A1 |
| 20110269109 | Miyazaki | Nov 2011 | A2 |
| 20110281251 | Mousques | Nov 2011 | A1 |
| 20110301620 | Di Betta et al. | Dec 2011 | A1 |
| 20120015337 | Hendrickson et al. | Jan 2012 | A1 |
| 20120015339 | Hendrickson et al. | Jan 2012 | A1 |
| 20120016362 | Heinrich et al. | Jan 2012 | A1 |
| 20120028231 | Misawa et al. | Feb 2012 | A1 |
| 20120045743 | Okano et al. | Feb 2012 | A1 |
| 20120065632 | Shadduck | Mar 2012 | A1 |
| 20120082970 | Pravong et al. | Apr 2012 | A1 |
| 20120100217 | Green et al. | Apr 2012 | A1 |
| 20120115117 | Marshall | May 2012 | A1 |
| 20120115118 | Marshall | May 2012 | A1 |
| 20120116391 | Houser et al. | May 2012 | A1 |
| 20120148994 | Hori et al. | Jun 2012 | A1 |
| 20120164616 | Endo et al. | Jun 2012 | A1 |
| 20120165866 | Kaiser et al. | Jun 2012 | A1 |
| 20120172873 | Artale et al. | Jul 2012 | A1 |
| 20120179072 | Kegreiss | Jul 2012 | A1 |
| 20120202180 | Stock et al. | Aug 2012 | A1 |
| 20120264096 | Taylor et al. | Oct 2012 | A1 |
| 20120264097 | Newcott et al. | Oct 2012 | A1 |
| 20120282583 | Thaler et al. | Nov 2012 | A1 |
| 20120282584 | Millon et al. | Nov 2012 | A1 |
| 20120283707 | Giordano et al. | Nov 2012 | A1 |
| 20120288839 | Crabtree | Nov 2012 | A1 |
| 20120308977 | Tortola | Dec 2012 | A1 |
| 20130087597 | Shelton, IV et al. | Apr 2013 | A1 |
| 20130101973 | Hoke et al. | Apr 2013 | A1 |
| 20130105552 | Weir et al. | May 2013 | A1 |
| 20130116668 | Shelton, IV et al. | May 2013 | A1 |
| 20130157240 | Hart et al. | Jun 2013 | A1 |
| 20130171288 | Harders | Jul 2013 | A1 |
| 20130177890 | Sakezles | Jul 2013 | A1 |
| 20130192741 | Trotta et al. | Aug 2013 | A1 |
| 20130218166 | Elmore | Aug 2013 | A1 |
| 20130224709 | Riojas et al. | Aug 2013 | A1 |
| 20130245681 | Straehnz et al. | Sep 2013 | A1 |
| 20130253480 | Kimball et al. | Sep 2013 | A1 |
| 20130267876 | Leckenby et al. | Oct 2013 | A1 |
| 20130282038 | Dannaher et al. | Oct 2013 | A1 |
| 20130288216 | Parry, Jr. et al. | Oct 2013 | A1 |
| 20130302771 | Alderete | Nov 2013 | A1 |
| 20130324991 | Clem et al. | Dec 2013 | A1 |
| 20130324999 | Price et al. | Dec 2013 | A1 |
| 20140011172 | Lowe | Jan 2014 | A1 |
| 20140017651 | Sugimoto et al. | Jan 2014 | A1 |
| 20140030682 | Thilenius | Jan 2014 | A1 |
| 20140038151 | Hart | Feb 2014 | A1 |
| 20140051049 | Jarc et al. | Feb 2014 | A1 |
| 20140072941 | Hendrickson et al. | Mar 2014 | A1 |
| 20140087345 | Breslin et al. | Mar 2014 | A1 |
| 20140087346 | Breslin et al. | Mar 2014 | A1 |
| 20140087347 | Tracy et al. | Mar 2014 | A1 |
| 20140087348 | Tracy et al. | Mar 2014 | A1 |
| 20140088413 | Von Bucsh et al. | Mar 2014 | A1 |
| 20140093852 | Poulsen et al. | Apr 2014 | A1 |
| 20140093854 | Poulsen et al. | Apr 2014 | A1 |
| 20140099858 | Hernandez | Apr 2014 | A1 |
| 20140106328 | Loor | Apr 2014 | A1 |
| 20140107471 | Haider et al. | Apr 2014 | A1 |
| 20140156002 | Thompson et al. | Jun 2014 | A1 |
| 20140162016 | Matsui et al. | Jun 2014 | A1 |
| 20140170623 | Jarstad et al. | Jun 2014 | A1 |
| 20140186809 | Hendrickson et al. | Jul 2014 | A1 |
| 20140187855 | Nagale et al. | Jul 2014 | A1 |
| 20140200561 | Ingmanson et al. | Jul 2014 | A1 |
| 20140212861 | Romano | Jul 2014 | A1 |
| 20140220527 | Li et al. | Aug 2014 | A1 |
| 20140220530 | Merkle et al. | Aug 2014 | A1 |
| 20140220532 | Ghez et al. | Aug 2014 | A1 |
| 20140242564 | Pravong et al. | Aug 2014 | A1 |
| 20140246479 | Baber et al. | Sep 2014 | A1 |
| 20140248596 | Hart et al. | Sep 2014 | A1 |
| 20140263538 | Leimbach et al. | Sep 2014 | A1 |
| 20140272878 | Shim et al. | Sep 2014 | A1 |
| 20140272879 | Shim et al. | Sep 2014 | A1 |
| 20140275795 | Little et al. | Sep 2014 | A1 |
| 20140275981 | Selover et al. | Sep 2014 | A1 |
| 20140277017 | Leimbach et al. | Sep 2014 | A1 |
| 20140303643 | Ha et al. | Oct 2014 | A1 |
| 20140303646 | Morgan et al. | Oct 2014 | A1 |
| 20140303660 | Boyden et al. | Oct 2014 | A1 |
| 20140308643 | Trotta et al. | Oct 2014 | A1 |
| 20140342334 | Black et al. | Nov 2014 | A1 |
| 20140349266 | Choi | Nov 2014 | A1 |
| 20140350530 | Ross et al. | Nov 2014 | A1 |
| 20140357977 | Zhou | Dec 2014 | A1 |
| 20140370477 | Black et al. | Dec 2014 | A1 |
| 20140371761 | Juanpera | Dec 2014 | A1 |
| 20140378995 | Kumar et al. | Dec 2014 | A1 |
| 20150031008 | Black et al. | Jan 2015 | A1 |
| 20150037773 | Quirarte Catano | Feb 2015 | A1 |
| 20150038613 | Sun et al. | Feb 2015 | A1 |
| 20150076207 | Boudreaux et al. | Mar 2015 | A1 |
| 20150086955 | Poniatowski et al. | Mar 2015 | A1 |
| 20150132732 | Hart et al. | May 2015 | A1 |
| 20150132733 | Garvik et al. | May 2015 | A1 |
| 20150135832 | Blumenkranz et al. | May 2015 | A1 |
| 20150148660 | Weiss et al. | May 2015 | A1 |
| 20150164598 | Blumenkranz et al. | Jun 2015 | A1 |
| 20150187229 | Wachli et al. | Jul 2015 | A1 |
| 20150194075 | Rappel et al. | Jul 2015 | A1 |
| 20150202299 | Burdick et al. | Jul 2015 | A1 |
| 20150209035 | Zemlock | Jul 2015 | A1 |
| 20150209059 | Trees et al. | Jul 2015 | A1 |
| 20150209573 | Hibner et al. | Jul 2015 | A1 |
| 20150228206 | Shim et al. | Aug 2015 | A1 |
| 20150262511 | Lin et al. | Sep 2015 | A1 |
| 20150265431 | Egilsson et al. | Sep 2015 | A1 |
| 20150272571 | Leimbach et al. | Oct 2015 | A1 |
| 20150272574 | Leimbach et al. | Oct 2015 | A1 |
| 20150272580 | Leimbach et al. | Oct 2015 | A1 |
| 20150272581 | Leimbach et al. | Oct 2015 | A1 |
| 20150272583 | Leimbach et al. | Oct 2015 | A1 |
| 20150272604 | Chowaniec et al. | Oct 2015 | A1 |
| 20150332609 | Alexander | Nov 2015 | A1 |
| 20150358426 | Kimball et al. | Dec 2015 | A1 |
| 20150371560 | Lowe | Dec 2015 | A1 |
| 20150374378 | Giordano et al. | Dec 2015 | A1 |
| 20150374449 | Chowaniec et al. | Dec 2015 | A1 |
| 20160000437 | Giordano et al. | Jan 2016 | A1 |
| 20160022374 | Haider et al. | Jan 2016 | A1 |
| 20160030240 | Gonenc et al. | Feb 2016 | A1 |
| 20160031091 | Popovic et al. | Feb 2016 | A1 |
| 20160058534 | Derwin et al. | Mar 2016 | A1 |
| 20160066909 | Baber et al. | Mar 2016 | A1 |
| 20160070436 | Thomas et al. | Mar 2016 | A1 |
| 20160073928 | Soper et al. | Mar 2016 | A1 |
| 20160074103 | Sartor | Mar 2016 | A1 |
| 20160098933 | Reiley et al. | Apr 2016 | A1 |
| 20160104394 | Miyazaki | Apr 2016 | A1 |
| 20160117956 | Larsson et al. | Apr 2016 | A1 |
| 20160125762 | Becker et al. | May 2016 | A1 |
| 20160133158 | Sui et al. | May 2016 | A1 |
| 20160140876 | Jabbour et al. | May 2016 | A1 |
| 20160194378 | Cass et al. | Jul 2016 | A1 |
| 20160199059 | Shelton, IV et al. | Jul 2016 | A1 |
| 20160220150 | Sharonov | Aug 2016 | A1 |
| 20160220314 | Huelman et al. | Aug 2016 | A1 |
| 20160225288 | East et al. | Aug 2016 | A1 |
| 20160232819 | Hofstetter et al. | Aug 2016 | A1 |
| 20160235494 | Shelton, IV et al. | Aug 2016 | A1 |
| 20160256187 | Shelton, IV et al. | Sep 2016 | A1 |
| 20160256229 | Morgan et al. | Sep 2016 | A1 |
| 20160262736 | Ross et al. | Sep 2016 | A1 |
| 20160262745 | Morgan et al. | Sep 2016 | A1 |
| 20160293055 | Hofstetter | Oct 2016 | A1 |
| 20160296144 | Gaddam et al. | Oct 2016 | A1 |
| Number | Date | Country |
|---|---|---|
| 2421706 | Feb 2001 | CN |
| 2751372 | Jan 2006 | CN |
| 2909427 | Jun 2007 | CN |
| 101313842 | Dec 2008 | CN |
| 101528780 | Sep 2009 | CN |
| 201364679 | Dec 2009 | CN |
| 201955979 | Aug 2011 | CN |
| 102458496 | May 2012 | CN |
| 202443680 | Sep 2012 | CN |
| 202563792 | Nov 2012 | CN |
| 202601055 | Dec 2012 | CN |
| 202694651 | Jan 2013 | CN |
| 103050040 | Apr 2013 | CN |
| 203013103 | Jun 2013 | CN |
| 203038549 | Jul 2013 | CN |
| 203338651 | Dec 2013 | CN |
| 203397593 | Jan 2014 | CN |
| 203562128 | Apr 2014 | CN |
| 102596275 | Jun 2014 | CN |
| 103845757 | Jun 2014 | CN |
| 103886797 | Jun 2014 | CN |
| 103396562 | Jul 2015 | CN |
| 105194740 | Dec 2015 | CN |
| 105504166 | Apr 2016 | CN |
| 9102218 | May 1991 | DE |
| 41 05 892 | Aug 1992 | DE |
| 44 14 832 | Nov 1995 | DE |
| 19716341 | Sep 2000 | DE |
| 1 024 173 | Aug 2000 | EP |
| 2 218 570 | Aug 2010 | EP |
| 2 691 826 | Dec 1993 | FR |
| 2 917 876 | Dec 2008 | FR |
| 2488994 | Sep 2012 | GB |
| 10 211160 | Aug 1998 | JP |
| 2001005378 | Jan 2001 | JP |
| 2009236963 | Oct 2009 | JP |
| 3162161 | Aug 2010 | JP |
| 2013127496 | Jun 2013 | JP |
| 101231565 | Feb 2013 | KR |
| PA 02004422 | Nov 2003 | MX |
| 106230 | Sep 2013 | PT |
| WO 199406109 | Mar 1994 | WO |
| WO 1996042076 | Dec 1996 | WO |
| WO 199858358 | Dec 1998 | WO |
| WO 199901074 | Jan 1999 | WO |
| WO 200036577 | Jun 2000 | WO |
| WO 200238039 | May 2002 | WO |
| WO 2002038039 | May 2002 | WO |
| WO 2004032095 | Apr 2004 | WO |
| WO 2004082486 | Sep 2004 | WO |
| WO 2005071639 | Aug 2005 | WO |
| WO 2006083963 | Aug 2006 | WO |
| WO 2007068360 | Jun 2007 | WO |
| WO 2008021720 | Feb 2008 | WO |
| WO 2008103383 | Aug 2008 | WO |
| WO 2009000939 | Dec 2008 | WO |
| WO 2009089614 | Jul 2009 | WO |
| WO 2010094730 | Aug 2010 | WO |
| WO 2011035410 | Mar 2011 | WO |
| WO 2011046606 | Apr 2011 | WO |
| WO 2011127379 | Oct 2011 | WO |
| WO 2011151304 | Dec 2011 | WO |
| WO 2012149606 | Nov 2012 | WO |
| WO 2012168287 | Dec 2012 | WO |
| WO 2012175993 | Dec 2012 | WO |
| WO 2013048978 | Apr 2013 | WO |
| WO 2013103956 | Jul 2013 | WO |
| WO 2014022815 | Feb 2014 | WO |
| WO 2014093669 | Jun 2014 | WO |
| WO 2014197793 | Dec 2014 | WO |
| WO 201 51 4881 | Oct 2015 | WO |
| WO 2016138528 | Sep 2016 | WO |
| WO 201 61 8341 | Nov 2016 | WO |
| WO 2016198238 | Dec 2016 | WO |
| WO 2016201085 | Dec 2016 | WO |
| WO 2017031214 | Feb 2017 | WO |
| WO 2017042301 | Mar 2017 | WO |
| Entry |
|---|
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2016/036664, entitled “Hysterectomy Model,” dated Dec. 21, 2017, 10 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2016/018697, entitled “Simulated Tissue Structures and Methods,” dated Aug. 31, 2017, 14 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2016/055148, entitled “Hysterectomy Model,” dated Apr. 12, 2018, 12 pgs. |
| European Patent Office, Examination Report for European Application No. 14733949.3 titled “Gallbladder Model,” dated Dec. 21, 2016, 6 pgs. |
| European Patent Office, The International Search Report and Written Opinion of the International Searching Authority for International Application No. PCT/US2016/062669 titled “Simulated Dissectible Tissue,” dated Apr. 5, 2017, 19 pgs. |
| European Patent Office, The International Search Report and Written Opinion of the International Searching Authority for International Application No. PCT/US2017/020389 titled “Simulated Tissue Cartridge”, dated May 24, 2017, 13 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability and Written Opinion for International Application No. PCT/US2015/059668, entitled “Simulated Tissue Models and Methods,” dated May 26, 2017, 16 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2018/018895, entitled “Synthetic Tissue Structures for Electrosurgical Training and Simulation,” dated May 17, 2018, 12 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2016/062669, entitled “Simulated Dissectible Tissue,” dated May 31, 2018, 11 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2018/018036, entitled “Laparoscopic Training System,” dated Jun. 8, 2018, 13 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2016/0032292, entitled “Synthetic Tissue Structures for Electrosurgical Training and Simulation,” dated Nov. 23, 2017, 2017, 8 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2016/034591, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Dec. 7, 2017, 2017, 14 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2017/039113, entitled “Simulated Abdominal Wall,” dated Aug. 7, 2017, 13 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2016/041852, entitled “Simulated Dissectible Tissue,” dated Jan. 25, 2018, 12 pgs. |
| European Patent Office, Extended European Search Report for European Patent Application No. EP 17202365.7, titled “Gallbladder Model”, dated Jan. 31, 2018, 8 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2016/043277, entitled “Appendectomy Model,” dated Feb. 1, 2018, 9 pgs. |
| European Patent Office, Invitation to Pay Additional Fees for International Application No. PCT/US2016/062669, titled “Simulated Dissectible Tissue”, dated Feb. 10, 2017, 8 pgs. |
| European Patent Office, The International Search Report and Written Opinion of the International Searching Authority for International Application No. PCT/US2016/055148 titled “Hysterectomy Model”, dated Feb. 28, 2017, 12 pgs. |
| Society of Laparoendoscopic Surgeons, “Future Technology Session: The Edge of Innovation in Surgery, Space, and Business,” http://www.laparoscopytoday.com/endourology/page/2/ , Figure 1B: http://laparoscopy.blogs.com/laparoscopy_today/images/6-1/6-1VlaovicPicB.jpg , Sep. 5-8, 2007, 10 pgs. |
| European Patent Office, International Search Report for International Application No. PCT/US2011/053859 A3, dated Apr. 5, 2012, entitled “Portable Laparoscopic Trainer,” 8 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2012/60997, entitled “Simulated Tissue Structure for Surgical Training,” dated Mar. 7, 2013, 8 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2012/070971, entitled “Advanced Surgical Simulation,” dated Mar. 18, 2013, 10 pgs. |
| Human Patient Simulator, Medical Education Technologies, Inc., http://www.meti.com (1999) all, printed Apr. 12, 2013, 24 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability and Written Opinion for International Application No. PCT/US2011/053859, entitled “Portable Laparoscopic Trainer,” dated Apr. 2, 2013, 9 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2013/062363, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Jan. 22, 2014, 11 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2013/061949, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Feb. 17, 2014, 7 pgs. |
| Anonymous: Realsim Systems—LTS2000, Sep. 4, 2005, pp. 1-2, XP055096193, Retrieved from the Internet: URL:https://web.archive.org/web/2005090403; 3030/http://www.realsimsystems.com/exersizes.htm (retrieved on Jan. 14, 2014). |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2013/062269, entitled “Surgical Training Model for Transluminal Procedures,” dated Feb. 17, 2014, 8 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2013/061557, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Feb. 10, 2014, 9 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2013/061728, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Oct. 18, 2013, 9 pgs. |
| Limps and Things, EP Guildford MATTU Hernia Trainer, http://limbsandthings.com/us/products/tep-guildford-mattu-hernia-trainer/, printed May 29, 2014, 11 pgs. |
| Simulab, Hernia Model, http://www.simulab.com/product/surgery/open/hernia model, printed printed May 29, 2014, 4 pgs. |
| McGill Laparoscopic Inguinal Hernia Simulator, Novel Low-Cost Simulator for Laparoscopic Inguinal Hernia Repair, Feb. 8, 2011, 1 pg. |
| University of Wisconsin-Madison Biomedical Engineering, Inguinal Hernia Model, http://bmedesign.engr.wisc.edu/projects/s10/hernia_model/, printed May 29, 2014, 62 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2012/070971, entitled “Advanced Surgical Simulation,” dated Jun. 24, 2014, 7 pgs. |
| European Patent Office, The International Search Report and Written Opinion of the International Searching Authority for International Application No. PCT/US2014/038195, entitled “Hernia Model”, dated Oct. 15, 2014, 20 pgs. |
| European Patent Office, The International Search Report and Written Opinion of the International Searching Authority for International Application No. PCT/US2014/048027, entitled “First Entry Model”, dated Oct. 17, 2014, 10 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2012/060997, entitled “Simulated Tissue Structure for Surgical Training” dated Apr. 22, 2014, 6 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2014/019840, entitled “Advanced Surgical Simulation Constructions and Methods,” dated Jul. 4, 2014, 8 pgs. |
| Kurashima, et al, “A tool for training and evaluation of Laparoscopic inguinal hernia repair; the Global Operative Assessment of Laparoscopic Skills-Groin Hernia” American Journal of Surgery, Paul Hoeber, New York, NY, US vol. 201, No. 1, Jan. 1 2011, pp. 54-61 XP027558745. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2014/042998, entitled “Gallbladder Model,” dated Jan. 7, 2015, 20 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability, for PCT application No. PCT/US2013/053497, entitled Simulated Stapling and Energy Based Ligation for Surgical Training, dated Feb. 12, 2015, 6 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2013/062363, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Apr. 9, 2015, 9 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2013/062269, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Apr. 9, 2015, 6 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2013/061557, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Apr. 9, 2015, 6 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2013/061728, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Apr. 9, 2015, 7 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2013/061949, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Apr. 9, 2015, 6 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2014/019840, entitled “Simulated Tissue Structure for Surgical Training,” dated Sep. 11, 2015, 8 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2015/020574, entitled “Advanced First Entry Model for Surgical Simulation,” dated Jun. 1, 2015, 12 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2015/022774, entitled “Simulated Dissectible Tissue,” dated Jun. 11, 2015, 13 pgs. |
| Anonymous: Silicone rubber-from Wikipedia, the free encyclopedia, pp. 1-6, XP055192375, Retrieved from the Internet: URL:http://en.wikipedia.org/w.index.php?title=Silicone_rubber&oldid=596456058 (retrieved on May 29, 2015). |
| Lamouche, et al., “Review of tissue simulating phantoms with controllable optical, mechanical and structural properties for use in optical coherence tomography,” Biomedical Optics Express, Jun. 1, 2012, 18 pgs., vol. 3, No. 6. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2014/038195, entitled “Hernia Model,” dated Nov. 26, 2015, 16 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2014/042998, entitled “Gallbladder Model,” dated Dec. 30, 2015, 15 pgs. |
| European Patent Office, International Search Report and Written Opinion for International Application No. PCT/US2013/053497, titled “Simulated Stapling and Energy Based Ligation for Surgical Training,” dated Nov. 5, 2013, 8 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2014/048027, entitled “First Entry Model,” dated Feb. 4, 2016, 8 pgs. |
| European Patent Office, International Search Report and Written Opinion for International Application No. PCT/US2015/059668, entitled “Simulated Tissue Models and Methods,” dated Apr. 26, 2016, 20 pgs. |
| Australian Patent Office, Patent Examination Report No. 1 for Australian Application No. 2012358851, titled “Advanced Surgical Simulation,” dated May 26, 2016, 3 pgs. |
| Miyazaki Enterprises, “Miya Model Pelvic Surgery Training Model and Video,” www.miyazakienterprises, printed Jul. 1, 2016, 1 pg. |
| European Patent Office, International Search Report and Written Opinion for International Application No. PCT/US2016/032292, entitled “Synthetic Tissue Structures for Electrosurgical Training and Simulation,” dated Jul. 14, 2016, 11 pgs. |
| European Patent Office, International Search Report and Written Opinion for International Application No. PCT/US2016/018697, entitled “Simulated Tissue Structures and Methods,” dated Jul. 14, 2016, 21 pgs. |
| European Patent Office, International Search Report and Written Opinion for International Application No. PCT/US2016/034591, entitled “Surgical Training Model for Laparoscopic Procedures,” dated Aug. 8, 2016, 18 pgs. |
| European Patent Office, The International Search Report and Written Opinion of the International Searching Authority for International Application No. PCT/US2016/036664, entitled “Hysterectomy Model”, dated Aug. 19, 2016, 15 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2015/020574, entitled “Advanced First Entry Model for Surgical Simulation,” dated Sep. 22, 2016, 9 pgs. |
| European Patent Office, The International Search Report and Written Opinion of the International Searching Authority for International Application No. PCT/US2016/0043277 titled “Appendectomy Model”, dated Oct. 4, 2016, 12 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2015/022774, titled “Simulated Dissectible Tissue,” dated Oct. 6, 2016, 9 pgs. |
| European Patent Office, The International Search Report and Written Opinion of the International Searching Authority for International Application No. PCT/US2016/041852 titled “Simulated Dissectible Tissue”, dated Oct. 13, 2016, 12 pgs. |
| 3D-MED Corporation, “Validated Training Course for Laparoscopic Skills,” https://www.3-dmed.com/sites/default/files/product-additional/product-spec/Validated%20Training%20Course%20Laparoscopic%20Skills.docx_3.pdf , printed Aug. 23, 2016, pp. 1-6. |
| 3D-MED Corporation, “Loops and Wire #1,” https://www.3-dmed.com/product/loops-and-wire-1 , printed Aug. 23, 2016, 4 pgs. |
| Barrier, et al., “A Novel and Inexpensive Vaginal Hysterectomy Simulatory,” Simulation in Healthcare: The Journal of the Society for Simulation in Healthcare, vol. 7, No. 6, Dec. 1, 2012, pp. 374-379. |
| European Patent Office, Extended European Search Report for European Patent Application No. EP 18184147.9, titled “First Entry Model,” dated Nov. 7, 2018, 7 pgs. |
| European Patent Office, Extended European Search Report for European Patent Application No. EP 18177751.7, titled “Portable Laparoscopic Trainer,” dated Jul. 13, 2018, 8 pgs. |
| European Patent Office, The International Search Report and Written Opinion for International Application No. PCT/US2018/034705, entitled “Laparoscopic Training System,” dated Aug. 20, 2018, 14 pgs. |
| The International Bureau of WIPO, International Preliminary Report on Patentability for International Application No. PCT/US2017/020389, entitled “Simulated Tissue Cartridge,” dated Sep. 13, 2018, 8 pgs. |
| Number | Date | Country | |
|---|---|---|---|
| 20160293055 A1 | Oct 2016 | US |
| Number | Date | Country | |
|---|---|---|---|
| 62119542 | Feb 2015 | US | |
| 62118179 | Feb 2015 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/US2016/018697 | Feb 2016 | US |
| Child | 15185360 | US |
