Abstract: A drug delivery device configured to simultaneously interface with a scala tympani and a scala vestibuli of a cochlea, wherein the device can be configured to deliver drug to the cochlea at least in part via a post introduction non-diffusion based delivery, and wherein the device can be configured to induce complete circuit circulation from the scala tympani to the scala vestibuli and/or vice versa, thereby distributing drug within the cochlea.

Abstract: Embodiments presented herein are generally directed to a perioperative implant cover configured to cover at least a portion of an implantable component during portions of the perioperative period (i.e., preoperative, intraoperative, and postoperative phases of surgery) in which the implantable component is susceptible to bacteria contamination. By covering the implantable component during these portions of the perioperative period, the cover reduces the possibility of bacteria contamination and subsequent perioperative colonization.

Abstract: Presented herein are implantable systems and methods for long-term delivery of treatment substance to a recipient.

Abstract: Presented herein are implantable systems and methods for long-term delivery of treatment substance to the ear of a recipient of an implantable auditory prosthesis.

Abstract: A locking member for a gate apparatus comprises a body mountable to a gripping array of a support, said body having a mating form mutually engageable with the gripping array, whereby axial motion of said body relative to said gripping array is inhibited. A member extends away from said body, said member defining a cross-tie mount for receiving a mating end of a cross-tie. The cross-tie mount has a cross-tie end retainer which is movable between a first position securing said cross-tie in said cross-tie mount, and a second position permitting release of said cross-tie from said cross-tie mount, whereby the cross-tie may be moved to function as a gate.

Abstract: A magnet is completely encased within a body of a biocompatible implant. The body of the biocompatible implant is formed so as to allow for removal of the magnet after implantation in a recipient. The body includes a portion that is at least partially separable from the remainder of the body, either by application of a removing agent or a tool. The magnet can be removed and replaced. Thereafter, the body can be sealed or the magnet can be left exposed.

Abstract: A magnet is completely encased within a body of a biocompatible implant. The body of the biocompatible implant is formed so as to allow for removal of the magnet after implantation in a recipient. The body includes a portion that is at least partially separable from the remainder of the body, either by application of a removing agent or a tool. The magnet can be removed and replaced. Thereafter, the body can be sealed or the magnet can be left exposed.

Abstract: A magnet is completely encased within a body of a biocompatible implant. The body of the biocompatible implant is formed so as to allow for removal of the magnet after implantation in a recipient. The body includes a portion that is at least partially separable from the remainder of the body, either by application of a removing agent or a tool. The magnet can be removed and replaced. Thereafter, the body can be sealed or the magnet can be left exposed.

Abstract: Presented herein are magnet arrangements for use with encapsulated implantable components. An implantable component comprises an implant body and a plurality of wire loops forming an internal coil that are encapsulated in a biocompatible overmolding. The implantable component also comprises a bone fixture positioned proximate to the plurality of wire loops and an implantable magnet attached to the bone fixture.

Abstract: A wear measurement system for a component is disclosed. The wear measurement system may include an imaging device configured to obtain a plurality of two-dimensional images of the component. The wear measurement system may also include a controller. The controller may be configured to generate a three-dimensional point cloud representing the component based on the two-dimensional images. The controller may also be configured to overlay a computer model of the component on the three-dimensional point cloud. Further, the controller may be configured to project the computer model on the two-dimensional images. The controller may also be configured to select at least two reference points appearing in each of a subset of images selected from the two-dimensional images. The controller may be configured to determine locations of the two reference points in the three-dimensional point cloud, determine an image distance between the locations, and determine an amount of wear based on the image distance.

Abstract: A wear measurement system for a component is disclosed. The wear measurement system may have an imaging device configured to obtain a plurality of two-dimensional images of the component. The wear measurement system may also have a controller. The controller may be configured to generate a three-dimensional point cloud representing the component based on the two-dimensional images. The controller may also be configured to select at least two reference points appearing in each of a subset of images selected from the two-dimensional images. Further, the controller may be configured to determine locations of the two reference points in the three-dimensional point cloud. The controller may also be configured to determine an image distance between the locations. In addition, the controller may be configured to determine an amount of wear based on the image distance.

Abstract: Embodiments are generally directed to a securable inner drug delivery plug or stopper that is configured to be inserted into, and secured (retained) within, an opening of the inner ear of an recipient. The securable inner drug delivery plug is configured to deliver drugs directly into the inner ear.

Abstract: Embodiments presented herein are generally directed to a perioperative implant cover configured to cover at least a portion of an implantable component during portions of the perioperative period (i.e., preoperative, intraoperative, and postoperative phases of surgery) in which the implantable component is susceptible to bacteria contamination. By covering the implantable component during these portions of the perioperative period, the cover reduces the possibility of bacteria contamination and subsequent perioperative colonization.

Abstract: A wear measurement system for a component is disclosed. The wear measurement system may include an imaging device configured to obtain a plurality of two-dimensional images of the component. The wear measurement system may also include a controller. The controller may be configured to generate a three-dimensional point cloud representing the component based on the two-dimensional images. The controller may also be configured to overlay a computer model of the component on the three-dimensional point cloud. Further, the controller may be configured to project the computer model on the two-dimensional images. The controller may also be configured to select at least two reference points appearing in each of a subset of images selected from the two-dimensional images. The controller may be configured to determine locations of the two reference points in the three-dimensional point cloud, determine an image distance between the locations, and determine an amount of wear based on the image distance.

Abstract: A wear measurement system for a component is disclosed. The wear measurement system may have an imaging device configured to obtain a plurality of two-dimensional images of the component. The wear measurement system may also have a controller. The controller may be configured to generate a three-dimensional point cloud representing the component based on the two-dimensional images. The controller may also be configured to select at least two reference points appearing in each of a subset of images selected from the two-dimensional images. Further, the controller may be configured to determine locations of the two reference points in the three-dimensional point cloud. The controller may also be configured to determine an image distance between the locations. In addition, the controller may be configured to determine an amount of wear based on the image distance.

Abstract: A locking member for a gate apparatus comprises a body mountable to a gripping array of a support, said body having a mating form mutually engageable with the gripping array, whereby axial motion of said body relative to said gripping array is inhibited. A member extends away from said body, said member defining a cross-tie mount for receiving a mating end of a cross-tie. The cross-tie mount has a cross-tie end retainer which is movable between a first position securing said cross-tie in said cross-tie mount, and a second position permitting release of said cross-tie from said cross-tie mount, whereby the cross-tie may be moved to function as a gate.

Abstract: Presented herein are implantable systems and methods for long-term delivery of treatment substance to the ear of a recipient of an implantable auditory prosthesis.

Abstract: A connector apparatus has a first portion and a second portion. The first portion mounts to an upright that has knobby hand grip protrusions. The second portion provides a connection for a laterally extending cross-member. The first portion interacts with the knobby hand grip protrusions to have a combination of a first degree of freedom permitting motion in one direction, while inhibiting motion in a second degree of freedom. The second portion has a releasable connection to the cross-member, and when engaged, has a degree of freedom of motion about an axis of the second portion cross-wise to the axis of the upright. The second portion has a releasable, retained, pin connector with a quarter-turn lock to prevent accidental disengagement. The connection of the second portion is offset such that when two connectors are seated back-to-back their cross-tie connections stand in substantially the same horizontal plane relative to the ground.

Abstract: Presented herein are implantable systems and methods for long-term delivery of treatment substance to the ear of a recipient of an implantable auditory prosthesis.

Abstract: An exercise device may comprise first and second elongated support members, at least one brace member for holding the first and second support members in a spaced apart relation to each other and a limb support device being disposed between the first and second support members and being interconnected thereto for sliding longitudinal relative to the first and second support members.