Abstract: According to a first aspect, a sound processor unit of a cochlear implant system is disclosed. The sound processor unit comprises an electric circuit, which comprises a sound processor antenna with a sound processor antenna capacitance and a sound processor antenna inductance, wherein the sound processor antenna capacitance and the sound processor antenna inductance are connected in series and form a resonant circuit.

Abstract: Presented herein are techniques for electronically locking an electronic device in response to detection of a safety critical fault. As used herein, a “safety critical fault” is a fault having a potential to cause harm to an individual using the device. In particular, an electronic device in accordance with certain embodiments presented herein is configured to determine when the electronic device has experienced a safety critical fault. In response, the electronic device automatically restarts itself and, following restart, is automatically forced into a locked mode. The locked mode prevents execution of a run-time program stored in the electronic device.

Abstract: An apparatus includes an enclosure containing a hermetically sealed region, the enclosure configured to be implanted on or within a recipient. The apparatus further includes circuitry within the hermetically sealed region and configured to generate signals. The apparatus further includes at least one heating element configured to receive the signals and to generate heat in response to the signals. The apparatus further includes at least one flow control element outside the hermetically sealed region and configured to respond to the heat by controlling a flow of liquid through at least one cannula to controllably administer the liquid internally to the recipient.

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: A device, including an electromagnetic transducer including a bobbin having a space therein, a connection apparatus in fixed relationship to the bobbin configured to transfer vibrational energy directly or indirectly at least one of to or from the electromagnetic transducer, and a passage from the space to the connection apparatus.

Abstract: An apparatus including an actuator and an electrode array support, wherein the apparatus is configured to insert an electrode array into a cochlea via controlled actuation of the actuator, wherein the controlled actuation is at least partially based on data that is at least partially based on electrical characteristics associated with the recipient.

Abstract: A system, including a central processor apparatus configured to receive input from a plurality of sound capture devices, wherein the central processor apparatus is configured to collectively evaluate the input from the plurality of sound capture devices to identify at least one spatial location that is more conducive to hearing with a hearing prosthesis relative to another spatial location.

Abstract: Presented herein are techniques for generating a hierarchical classification of a set of sound signals received at hearing prosthesis. The hierarchical classification includes a plurality of nested classifications of a sound environment associated with the set of sound signals received at hearing prosthesis, including a primary classification and one or more secondary classifications that each represent different characteristics of the sound environment. The primary classification represents a basic categorization of the sound environment, while the secondary classifications define sub-categories/refinements of the associated primary classification and/or other secondary classifications.

Abstract: Providing stimulation signals for an implanted auditory prosthesis including receiving first and second sound signals at first and second sound input devices, each of the first and second signals having a signal-to-noise ratio; determining a signal parameter related to said signal-to-noise ratio of each of the first and second signals; selecting one of the first and second signals which has the greater signal-to-noise ratio; and generating stimulation signals for the implanted auditory prosthesis based on said selected sound signal.

Abstract: A method, including an action of receiving first data based on data based on ambient sound captured with a first microphone, and further including an action of receiving second data based on data based on the ambient sound captured with a second microphone, wherein the first microphone is a part of a hearing prosthesis, the second microphone is part of an indoor sound capture system or indoor sound capture sub-system, and the method further comprises comparing the first data to the second data.

Abstract: Examples disclosed herein are relevant to a wearable device configured to selectively receive a primary magnet set selected from among multiple primary magnet sets of varying magnetic strengths. A supplemental magnet set is used with the wearable device to supplement the selected primary magnet set to increase a strength of a magnetic connection. The wearable device can selectively couple with a selected cover. The cover can be an accommodating cover configured to accommodate the at least one supplemental magnet set or a non-accommodating cover for use as the selected cover when a supplemental magnet set is not being used.

Abstract: Embodiments presented herein are generally directed to techniques for separately transferring power and data from an external device to an implantable component of a partially or fully implantable medical device. The separated power and data transfer techniques use a single external coil and a single implantable coil. The external coil is part of an external resonant circuit, while the implantable coil is part of an implantable resonant circuit. The external coil is configured to transcutaneously transfer power and data to the implantable coil using separate (different) power and data time slots. At least one of the external or internal resonant circuit is substantially more damped during the data time slot than during the power time slot.

Abstract: A method, including receiving a signal which includes speech data, processing the received signal to identify and/or predict one or more words in the speech data, and evoking a hearing percept based on the received signal, wherein the evoked hearing percept includes one or more modified words based on the identification and/or prediction of the one or more words.

Abstract: A prosthetic system, comprising a first sub-system configured to evoke a hearing percept based on a first principle of operation, and a second sub-system configured to evoke a hearing percept based on at least one of the first principle of operation or a second principle of operation different from the first principle of operation, wherein the first and second sub-systems are configured to independently process respective inputs indicative of an ambient sound to harmonize an estimated recipient perception of magnitude of a property of the respective evoked hearing percepts.

Abstract: Technologies disclosed herein can be used to provide power and data to an implantable device implanted in a recipient, such as when the recipient is not wearing an external device. An example system includes a pillow or other headrest configured as a power and data source for an implanted medical device. Disclosed technologies can be configured to continuously provide power and data to an implantable medical devices over a period of time, such as substantially the entire period of time where the recipient is resting their head on the pillow.

Abstract: Examples disclosed herein are relevant to monitoring and treating sensory conditions affecting an individual. Sensors and intelligence integrated within a sensory prosthesis (e.g., an auditory prosthesis) can automatically obtain objective data regarding the ability of one or more of an individuals senses during day-to-day activities. A treatment action can be taken based on the objective data. Further disclosed herein are techniques relating to reducing the gathering of irrelevant sensory input and automatically transmitting relevant data to a caregiver device.

Abstract: Techniques for locating a misplaced primary wireless device (within a spatial region. In particular, the techniques presented herein use a secondary wireless device to collect a plurality of multivariate wireless data points within the spatial region. An artificially intelligent search algorithm analyzes the plurality of multivariate wireless data points to estimate the location of the wireless device. Directional instructions that guide the user to the estimated location of the primary wireless device are generated and then provided to the user.

Abstract: Disclosed examples include technology for the detection and treatment of neotissue formation proximate an implantable stimulator. Neotissue formation can include ossification, scar tissue, soft tissue fibrosis, and other tissue growth. The neotissue formation can be detected by analyzing (e.g., using a machine-learning framework) stimulation data relating to the implantable stimulator. Neotissue formation characteristics can be analyzed to determine appropriate treatment actions for ameliorating the effects of neotissue formation.

Abstract: Examples disclosed herein are relevant to improvements in connectors for bone conduction devices, particularly bone conduction auditory prostheses, to connect to an abutment. Disclosed examples include a connector assembly having a vibration conductor separate from a coupling. Examples can further include an adapter to modify a length of the connector assembly. Examples can further provide an angled connector assembly to modify an angle at which the connector assembly connects to an abutment.

Abstract: An apparatus is provided which includes a biocompatible housing configured to be implanted within a recipient. The housing includes a unitary wall including a first wall portion and a second wall portion surrounding a perimeter of the first wall portion. The first wall portion is sufficiently flexible to transmit vibrations between an outer region outside the housing and an inner region within the housing.