The present invention is directed to a wearable system wherein elements of the system, including various sensors adapted to detect biometric and other data and/or to deliver drugs, are positioned proximal to, on the ear or in the ear canal of a person. In embodiments of the invention, elements of the system are positioned on the ear or in the ear canal for extended periods of time. For example, an element of the system may be positioned on the tympanic membrane of a user and left there overnight, for multiple days, months, or years. Because of the position and longevity of the system elements in the ear canal, the present invention has many advantages over prior wearable biometric and drug delivery devices.

A device for securing an external transmitter of a cochlear implant to the head of the wearer. A pouch containing the external transmitter is secured using a plurality of straps coupled to a decorative shell worn on a person's head. The pouch and the decorative shell are designed to allow sound to pass unhindered from the environment to the inner ear. The plurality of straps are adjustable to allow precise placement of the external transmitter over the internal receiver. The external transmitter is also secured using a pouch coupled to a decorative shell. The external transmitter is further secured using a sealer coupled to the transmitter and further coupled to the head using an adhesive barrier. The sealer is made of a semi-transparent material. The device ensures that an external transmitter remains in place.

Presented herein are hybrid multi-phasic stimulation techniques for stimulation of tissue of a recipient of an implantable medical device. In particular, in accordance with the hybrid multi-phasic stimulation techniques, at least one stimulation current pulse is delivered to the tissue of the recipient in order to stimulate the tissue. The at least one stimulation current pulse injects charge into the tissue that is then removed through the combination of at least one discharging current pulse and a period of electrode shorting.

Presented herein are techniques for providing tinnitus relief to recipients via an implantable arrangement. In accordance with embodiments presented herein, an implantable medical device, such as implantable tinnitus therapy device, auditory/hearing prosthesis, etc., comprises one or more implantable sensors configured to be implanted in a recipient. The one or more implantable sensors are configured to detect body noises of the recipient. The implantable medical device is configured to classify/categorize the one or more body noises and set, select, or otherwise determine a tinnitus therapy for the recipient based on the classification of the one or more body noises.

A system including a cochlear implant with a cochlear lead including a plurality of electrodes, an antenna, a stimulation processor operably connected to the antenna and to the cochlear lead, and a magnet apparatus, adjacent to the antenna, including a case defining a central axis, a frame within the case and rotatable relative to the case about the central axis of the case, and only two elongate diametrically magnetized magnets that are located in the frame, that are separated from one another by a fixed non-zero distance, that each define a longitudinal axis and a N-S direction, and that are rotatable about the longitudinal axis relative to the frame, and an external device including an axially magnetized disk-shaped positioning magnet and an antenna adjacent to the axially magnetized disk-shaped positioning magnet.

Disclosed examples generally include methods and apparatuses related to microphone units, such as may be found in implantable medical devices (e.g., cochlear implants). Microphone units generally include a microphone element connected to a chamber having a concave floor with the chamber covered by a membrane. Microphone units can be configured to produce an output based on pressure waves (e.g., sound waves) that reach the membrane. In an example, a microphone unit has a pressurized gas within the chamber below the membrane such that, while in a static state, the membrane deflects away from the chamber floor.

A hearing prosthesis, comprising: a microphone; a sound processor; an external transmitter unit including a coil; an internal receiver unit including a coil; a stimulator unit, wherein the stimulator unit includes a control circuit, a voltage measurement component, a resistor and a signal generator, wherein the measurement circuit is configured to output a signal indicative of the voltage across the resistor; and a stimulating lead assembly array, wherein at least a portion of the hearing prosthesis is configured to apply an electrical signal to tissue inside a cochlea of a recipient, and at least a portion of the hearing prosthesis is configured to sense an electrical property inside of the cochlea that results from the applied electrical signal and the interaction of the applied electrical signal to the tissue.

An apparatus includes a housing configured to be placed over a portion of skin of a recipient, the portion of skin overlaying an implanted device. The apparatus further includes circuitry within the housing. The circuitry is configured to wirelessly communicate with the implanted device. The apparatus further includes a unitary magnet in mechanical communication with the housing. The magnet includes at least one first magnetic dipole moment having a first magnitude and a first direction and at least one second magnetic dipole moment having a second magnitude substantially equal to the first magnitude and a second direction substantially opposite to the first direction.

An apparatus includes a cannula with at least one wall portion having an electrically insulating material. The at least one wall portion at least partially bounds a region configured to contain a portion of a medical implant system configured to be implanted on or within a recipient. The cannula further includes at least one portion configured to provide at least one electrically conductive pathway through the at least one wall portion from within the cannula to a region outside the cannula.

Presented herein are techniques that make use of objective measurements obtained in response to acoustic stimulation signals. More specifically, at least one measure of outer hair cell function and at least one measure of auditory nerve function are obtained from a tonotopic region of an inner ear of a recipient of a hearing prosthesis. The at least one measure of auditory nerve function and the least one measure of outer hair cell function are then analyzed relative to one another.