This application is the U.S. National Stage of PCT App. Ser. No. PCT/EP2013/050456, filed Jan. 11, 2013.
The present invention relates to shells for hearing devices. Hearing devices include hearing aids for the hard of hearing, communication devices, and active hearing protection for loud noises. They are at least partially positioned in the wearer's ear to varying degrees, and may incorporate a behind-the-ear unit situated behind the wearer's pinna and connected either acoustically or electrically with an earpiece.
Currently, shells for hearing devices, that is to say the outer shell of an In-the-Ear hearing device or the shell of an earpiece of a Behind-The-Ear hearing device, are in general constructed as a hard shell shaped according to an impression or scan taken of the individual's unique ear canal in a static jaw position. Since the shape of the ear canal varies during normal jaw movement e.g. when talking or chewing, pressure can be exerted by the hard shell of the hearing device on the ear canal, leading to discomfort, sound leakage during jaw movement, and possible generation of disturbing noises when speaking or eating. Furthermore, the hearing device or earpiece may also migrate out of the wearer's ear due to these dynamic changes in ear canal geometry.
Various prior art attempts to mitigate these problems have been disclosed in U.S. Pat. No. 7,720,242, US 2004/0252854 and U.S. Pat. No. 7,130,437, however the resulting hearing devices are somewhat bulky and are thus little suited for modern so-called “Invisible In the Canal (iiC)” applications, which are inserted deep into the ear canal and extending into the bony region, and therefore require a high level of miniaturisation.
The aim of the present invention is thus to overcome at least some of the disadvantages of the prior art.
The object of the invention is attained by a shell for a hearing device, which comprises a sub-shell comprising one or more lateral openings, and a thermoformed hull attached to the subshell and covering the one or more lateral openings. “Lateral” should be understood as “sideways” or “transverse”, i.e. the opening(s) is/are situated in the side of the sub-shell, a normal to a plane tangential to the centroid of the opening being at an angle to the major axis of the sub-shell. Particularly, this angle is greater than 30°.
In consequence, in the region of the lateral opening or openings, the local rigidity of the shell is reduced, since the local rigidity is only that of the thermoformed hull. On the remainder of the shell, the rigidity is that of the sum of the rigidities of the sub-shell and of the thermoformed hull. In consequence, the local rigidity can be substantially reduced in comparison to single-piece and/or single-material shells e.g. in the regions of the shell subject to pressure from the ear canal during dynamic movement thereof, such as during chewing, talking etc. Due to this reduction in local rigidity, the local flexibility is likewise increased, permitting the shell to flex and deform in response to ear canal movement, reducing discomfort for the wearer. In dimensional terms, the total thickness of the shell can be reduced to 0.1 mm or less, or even down to 20 μm, in the region of the openings in the sub-shell, while the total thickness of the shell can remain at 0.4 mm or greater outside of the region of the openings in the sub-shell, ensuring that the shell as a whole exhibits sufficient rigidity and mechanical stability. With current manufacturing techniques, this is not achievable with a single-piece and/or single-material shell.
In an embodiment, the sub-shell is more rigid than the thermoformed hull, ensuring that the shell as a whole exhibits sufficient resistance to excessive longitudinal deformation of the shell.
In an embodiment, the at least one lateral opening is situated at a location on the sub-shell destined to be subject to pressure due to dynamic changes in the shape of the ear canal of the wearer e.g. during normal jaw movement, the opening or openings being shaped so as to permit the thermoformed hull to flex in response to this pressure. Thus, the wearer's comfort is enhanced.
In an embodiment, the at least one lateral opening comprises at least two lateral openings situated in substantially opposite side of the sub-shell, i.e. substantially facing each other across the interior cavity of the shell. This optimises the location of the less rigid, more flexible shell regions to better respond to changes in the shape of the wearer's ear canal.
In an embodiment, the shell comprises a vent channel formed between the thermoformed hull and the groove provided in the sub-shell. This eliminates the requirement for a separate vent tube passing through the interior of the shell, saving space in the interior of the shell for electronic components. Furthermore, since this vent channel is closed along its length and just open at its extremities, it is less susceptible to cerumen buildup than for instance an open vent channel or groove formed in the outer surface of the shell. Additionally, forming the vent channel by a groove in the sub-shell on the one side and the thermoformed hull on the other side, construction is easier than closed channels formed in the wall thickness of a single-piece shell.
In an embodiment, the sub-shell is situated on the interior of the thermoformed hull, giving a continuous, smooth outer surface to the shell and allowing the openings in the sub-shell to free up space on the interior of the shell for placement of electronic components.
In an alternative embodiment, the sub-shell is situated on the exterior of the thermoformed hull, protecting the bulk of the thermoformed hull from damage.
In an embodiment, the thermoformed hull is made of PE (Polyethylene), BAREX (Acrylonitrile/Methyl acrylate), PET (Polyethylene Terephthalate), COP (Cyclo Olefin Polymer), PCTFE (Polychlortrifluorethylene), EVA (Ethylene-vinyl acetate) or PEEK (Polyetheretherketone). These materials are all thermoformable materials with the requisite properties, for instance tensile strength, moisture barrier properties, chemical resistance, and biocompatibility. The sub-shell is constructed of a polymer material or a ceramic-filled polymer material such as UV- or visible light cured acrylic resins which are already used for the generative/additive manufacturing of hearing aid shells. Alternatively, the sub-shell can also be made of a sintered thermoplastic polymer powder (e.g. polyamide PA12). These materials are suitable for use with generative manufacturing methods, have the requisite stiffness and strength, chemical resistance and are biocompatible.
The object of the invention is likewise attained by a hearing device comprising a shell as described above.
Furthermore, the object of the invention is attained by a method of manufacturing a shell for a hearing device. This method comprises manufacturing a sub-shell which comprises at least one lateral opening. A thermoformed hull conformed to fit the sub-shell is formed, either separately, or in situ, and the hull is attached to the sub-shell so that the thermoformed hull covers the at least one lateral opening. The attachment may take place by forming the thermoformed hull and the sub-shell integrally, or may take place separately e.g. by adhesive bonding, ultrasonic welding, or similar.
Thereby, a shell for a hearing device is formed in which, in the region of the lateral opening or openings, the local rigidity of the shell is reduced, since the local rigidity is only that of the thermoformed hull. On the remainder of the shell, the rigidity is that of the sum of the rigidities of the sub-shell and of the thermoformed hull. In consequence, the local rigidity of the shell can be substantially reduced e.g. in the regions of the shell subject to pressure from the ear canal during dynamic movement thereof, such as during chewing, talking etc. Due to this reduction in local rigidity, the local flexibility is likewise increased, permitting the shell to flex and deform in response to ear canal movement, reducing discomfort for the wearer. In dimensional terms, the total thickness of the shell can be reduced to 0.1 mm or less, or even down to 20 μm, in the region of the openings in the sub-shell, while the total thickness of the shell can remain at 0.4 mm or greater outside of the region of the openings in the sub-shell, ensuring that the shell as a whole exhibits sufficient rigidity and mechanical stability. With current manufacturing techniques, this is not achievable with a single-piece shell formed by injection moulding, or by generative manufacturing methods.
In an embodiment of the method, the hull is formed by taking at least two measurements of an ear canal of a patient e.g. at different jaw positions, and then fabricating a thermoforming die based at least partially on these measurements, e.g. by computer modelling of an optimal shell form and deriving from this modelling the required shape of the thermoformed hull. Subsequently, the thermoformed hull is thermoformed by means of the thermoforming die. Thus, a precise, custom-shaped thermoformed hull is created.
In an embodiment of the method, the thermoforming die is formed by a generative manufacturing process such as laser sintering, laser lithography, stereolithography, or a thermojet process. This enables cost-effective manufacturing of a custom thermoforming die.
In an embodiment of the method, the sub-shell is formed by modification of the thermoforming die after thermoforming of the thermoformed hull. This removes the necessity to manufacture the sub-shell separately, keeping production costs low, and, since the sub-shell is made from the thermoforming die, the fit between the sub-shell and the thermoformed hull is extremely precise. Furthermore, by means of this method, the sub-shell and the thermoformed hull may be formed integrally with each other. In a further embodiment of the method, the hull is attached to the thermoforming die during the step of thermoforming of the thermoformed hull, and the step of forming the sub-shell comprises removing portions of the thermoforming die, such as weakened break-away “windows”, to form the sub-shell. This speeds up the process of converting the thermoforming die to the sub-shell, since such easily-removable portions can be removed with little effort.
In an alternative embodiment of the method, the thermoforming die is constituted at least partially by the sub-shell. This has the advantage that no separate thermoforming die need be produced, keeping costs low and ensuring excellent fit between the thermoformed hull and the sub-shell. Furthermore, by means of this method, the sub-shell and the thermoformed hull may be formed integrally with each other.
In an embodiment of the method, the sub-shell is formed by taking at least two measurements of an ear canal of a patient e.g at different jaw positions, then, based at least partially on these measurements, e.g. by computer modelling of an optimal shell form and deriving from this modelling the required shape of the sub-shell, forming the sub-shell by means of a generative manufacturing process such as laser sintering, laser lithography, stereolithography, or a thermojet process. This enables cost-effective manufacturing of a sub-shell.
In an embodiment of the method, the thermoformed hull is attached on the exterior of the sub-shell, giving a continuous, smooth outer surface to the shell and allowing the openings in the sub-shell to free up space on the interior of the shell for placement of electronic components. Alternatively, the thermoformed hull is attached on the interior of the sub-shell, leaving the sub-shell exposed and thereby protecting the bulk of the thermoformed hull from damage.
In an embodiment of the method, the thermoformed hull is made of PE (Polyethylene), BAREX (Acrylonitrile/Methyl acrylate), PET (Polyethylene Terephthalate), COP (Cyclo Olefin Polymer), PCTFE (Polychlortrifluorethylene), EVA (Ethylene-vinyl acetate) or PEEK (Polyetheretherketone) these materials are all thermoformable materials with the requisite properties, for instance tensile strength, moisture barrier properties, and biocompatibility. The sub-shell is constructed of a polymer material or a ceramic-filled polymer material such as UV- or visible light cured acrylic resins which are already used for the generative/additive manufacturing of hearing aid shells. Alternatively, the sub-shell can also be made of a sintered thermoplastic polymer powder (e.g. PA12). These plastics are suitable for use with generative manufacturing methods, have the requisite stiffness and strength, and are biocompatible.
The object of the invention is likewise attained by a method of manufacturing a hearing device, comprising manufacturing a shell according to one of the above-mentioned methods, further comprising the step of assembling at least one further hearing device component into the shell, thereby applying the shell of the invention to a complete hearing device.
In an embodiment of the method of manufacturing a hearing device, the at least one further hearing device component comprises an electronic module, and the faceplate is furthermore assembled to the open end of the shell. The shell of the invention is thus built into an in-the-ear-type hearing device.
In an alternative embodiment of the method of manufacturing a hearing device, the further hearing device component comprises at least one of a receiver and a sound tube, incorporating the shell of the invention into a behind-the-ear hearing device.
The invention will now be further elaborated by means of the attached figures, which show:
In the figures, like parts and like method steps are represented by like reference signs.
Sub-shell 11 is fabricated of a relatively rigid biocompatible material, such as a polymer material or a ceramic-filled polymer material such as UV- or visible light cuarble acrylic resins, and is responsible for the majority of the structural integrity and stiffness of the shell 10. As such, the wall thickness of the sub-shell 11 would typically be at least 0.4 mm to ensure this structural stability, however this value is not to be construed as limiting. Furthermore, sub-shell 11 comprises lateral openings 13 in the sides of the sub-shell 11, which will be described in greater detail below.
Thermoformed hull 12 is fabricated of a relatively flexible biocompatible thermoformable polymer film such as PE (Polyethylene), BAREX (Acrylonitrile/Methyl acrylate), PET (Polyethylene Terephthalate), COP (Cyclo Olefin Polymer), PCTFE (Polychlortrifluorethylene), EVA (Ethylene-vinyl acetate) or PEEK (Polyetheretherketone), and ideally has a wall thickness of less than 0.1 mm. Thicknesses as low as 20 μm are today possible. In consequence, the wall thickness of the complete shell is locally reduced to 0.1 mm or less, rendering the shell flexible in the region of lateral openings 13 and thus able to flex in response to changes in ear canal geometry without resulting in excess pressure being applied to the ear canal. The thermoformed hull 12 is furthermore responsible for acting as a barrier for preventing moisture, cerumen, dust, and so on from entering the interior of the shell 10.
Thermoformed hulls 12 are easily distinguishable from hulls or shells produced by other processing techniques such as injection moulding. Firstly, thermoforming enables the wall thickness of the thermoformed hull 30 to be significantly thinner (approximately 50-100 μm, or even 20-100 μm thickness) than those produced e.g. by injection moulding: injection moulded shells or hulls are typically 3 to 5 times thicker due limitations of the process. As a result, they are relatively rigid, and either exhibit visible seams and/or sprues, or must be created as two half-shells, such as that described in U.S. Pat. No. 7,092,543. Since the thermoformed hulls have significantly thinner walls than injection moulded hulls, or hulls produced by other methods, they are relatively elastic and flexible. Secondly, the orientation of the crystal structure of the plastic material is identifiably different in a thermoformed hull compared with an injection moulded hull. Despite the relatively thin wall thickness, thermoformed hulls retain very high tensile strength.
As was briefly stated above, sub-shell 11 comprises lateral openings 13 in the sides of the sub-shell 11, which are covered by the thermoformed hull 12 when the shell 10 is assembled. These openings 13 are provided in locations in the shell 10 which will be subject to pressure from the ear canal as it changes shape e.g. during jaw movement. These openings 13 are covered by the thermoformed hull 12 to prevent ingress of moisture, cerumen, dust etc. into the interior of the shell 10, and so as to render the area of each opening 13 more flexible than the remainder of the sub-shell 11. Essentially, the local stiffness of the shell 10 is the sum of the stiffness of the sub shell 11 and the stiffness of the thermoformed hull 12 at all points where sub-shell material is present, which prevents excessive longitudinal deformation of the shell 10, provides resistance to crushing, e.g. from mishandling, and protection from damage e.g. when dropped. In the region of the openings 13, the local stiffness of the shell 10 is only that of the thermoformed hull 12, which is flexible in comparison to the sub-shell 11. This locally reduced stiffness enables the shell 10 to easily deform in response to pressure in the area of the openings 13, thus allowing the shape of the shell 10 to adapt to movements of the ear canal of the wearer, reducing wearer discomfort. Furthermore, in the region of the openings 13 there is more volume available inside the shell 10 for hearing device components than there would be if the openings 13 were not present.
It is naturally also foreseeable to incorporate a vent tube of this type into the second embodiment of
As previously discussed, any of the shells 10, 20, 30, 40, can form at least part of the enclosure of an in-the-ear hearing device, or at least part of an earpiece for a behind-the-ear hearing device. In the former case, the hearing device itself is at least partially disposed within the shell, and in the latter case, the shell is connected to the main body of the hearing device either via a sound tube in the case in which the receiver (loudspeaker) is situated in the behind-the-ear unit, or via an electrical wire in the case in which the receiver (loudspeaker) is situated in the shell rather than in the behind-the-ear unit.
A hearing device so constructed presents several options for applying serial numbers. The serial number may be engraved e.g. by laser on the sub-shell, visible through the thermoformed hull, or on the thermoformed hull itself, with or without application of coloured lacquer.
Firstly, in step 90, at least two measurements are made of a patient's ear canal at different jaw opening positions so as to ascertain the shape of the ear canal during natural movements. This can be performed by means of one or more of the following techniques:
Once the at least two measurements have been made, in step 91, the gathered data are then used to model the optimal form of the sub-shell and the thermoformed hull which will together constitute the shell. This modelling takes into account the structural stiffness required, as well as the position and size of openings in the sub-shell to compensate for changes in the shape of the ear canal during jaw movement. Any further features such as a groove for a vent tube such as that illustrated in
Following now along the upper track of
In step 93, polymer film 203, which may be of a material such as PE, BAREX, PET, COP PCTFE, EVA or PEEK, and may have a wall thickness of less than 0.1 mm, is vacuum thermoformed over thermoforming mould 200, with the assistance of a vacuum applied via baseplate 202, as is conventional and thus need not be described further. Subsequently, in step 94 the now thermoformed polymer film 204, having taken the shape of the thermoforming die 200, is removed from the thermoforming die 200, e.g. by applying a positive pressure via baseplate 202, or simply by pulling the thermoformed polymer film 204 from the die, as is conventional. In step 95, the thermoformed hull 205 is liberated from the excess thermoformed polymer film 204e, e.g. by laser cutting, hot wire cutting, or mechanical cutting such as with an ultrasonic knife. Advantageously, this cutting may take place in the plane of the faceplate. At this stage, if desired, holes for e.g. a sound outlet, wax guard etc may be formed in the thermoformed hull 205 by e.g. laser cutting, either before, during, or after liberation of the thermoformed hull 205 from the remainder of the thermoformed polymer film.
Following now the lower track of
Once both the thermoformed hull 205 and the sub-shell 206 have been fabricated, the sub-shell 206 is inserted into thermoformed hull 205, and they are bonded together. This bonding can take place by any known method, such as by applying adhesive to one or more of the thermoformed hull 205 and the sub-shell 206, or by welding, e.g. ultrasonic welding.
The shell 207 is thus in principle completed in step 98, and any required holes for e.g. a sound outlet, wax guard etc. if desired can be drilled at this stage, either mechanically or by laser cutting.
The shell is then ready to be assembled into a completed hearing device, i.e. in the case of an in-the-ear hearing device, the electronics module and faceplate can be assembled to the shell, or in the case of a behind-the-ear hearing device, a sound tube, or a loudspeaker and electric cable can be assembled into the shell. This applies equally to the completed shells of any of the below embodiments.
Steps 90, 91 and 96 are identical to those of
However, following the upper path of
Following now the lower track of
The shell is then ready to be assembled into a completed hearing device as described above.
Dealing first with the steps common to both the third and the fourth embodiments, steps 90-94 are the same as those of
The third embodiment of the method is represented by the upper track, labelled “A”, on
Turning now to the fourth embodiment of the method as represented by the lower track, labelled “B” on
It should be noted that, although the third and fourth embodiments illustrated in
Steps 90, 91 and 96 are the same as in the embodiment of
In step 115, the thermoformed polymer film 204 is removed from the base plate 202 together with the sub-shell 206, and in step 116, the excess thermoformed film 204e is removed by e.g. laser cutting, hot wire cutting, or mechanical cutting such as with an ultrasonic knife. The shell 207 can then be finished as in previous embodiments, and is ready to be assembled into at least part of a hearing device.
Although the foregoing embodiments illustrate the manufacture of the shell in terms of custom shell design fitted to one individual, the invention is equally applicable to off-the-shelf standard shells. In such a case, steps 90 and 91 are omitted, and previously-defined standard sub-shells 206 and standard thermoformed hulls 205 are produced. Defining standard shells can for instance be carried out by taking the measurements of step 90 of a large number of individuals, and mathematically defining “best fit” shell models.
Furthermore, application of a serial number to the shell, either on the sub-shell or the thermoformed hull, may be carried out at any convenient point in any of the above-mentioned methods.
Although the invention has been described in terms of specific embodiments, these are not be construed as limiting to the invention, which is solely defined by the scope of the appended claims.
Filing Document | Filing Date | Country | Kind |
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PCT/EP2013/050456 | 1/11/2013 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
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WO2014/108200 | 7/17/2014 | WO | A |
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PCT Search Report dated Sep. 20, 2013 for PCT App. Ser. No. PCT/EP2013/050456. |
Number | Date | Country | |
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20150358749 A1 | Dec 2015 | US |