Abstract: A magnetic system for a medical implant system is described. A planar implant receiver coil is configured to lie underneath and parallel to overlying skin of an implanted patient for transcutaneous communication of an implant communications signal. A planar ring-shaped attachment magnet also is configured to lie underneath and parallel to the overlying skin and radially surrounds the receiver coil. The attachment magnet is characterized by a magnetic field configured to avoid creating torque on the attachment magnet in the presence of an external magnetic field.

Abstract: A magnetic system for a medical implant system is described. A planar implant receiver coil is configured to lie underneath and parallel to overlying skin of an implanted patient for transcutaneous communication of an implant communications signal. A planar ring-shaped attachment magnet also is configured to lie underneath and parallel to the overlying skin and radially surrounds the receiver coil. The attachment magnet is characterized by a magnetic field configured to avoid creating torque on the attachment magnet in the presence of an external magnetic field.

Abstract: A magnetic system for a medical implant system is described. A planar implant receiver coil is configured to lie underneath and parallel to overlying skin of an implanted patient for transcutaneous communication of an implant communications signal. A planar ring-shaped attachment magnet also is configured to lie underneath and parallel to the overlying skin and radially surrounds the receiver coil. The attachment magnet is characterized by a magnetic field configured to avoid creating torque on the attachment magnet in the presence of an external magnetic field.

Abstract: A fluid delivery system for delivering fluid to an inner ear of a subject includes a septum configured to be embedded in the inner ear or on a promontory bone of the subject, a spear connector having a needle for insertion into the septum, a catheter in fluid communication with the spear connector, a fixation device configured to secure the septum to the inner ear or the promontory bone.

Abstract: A fluid delivery system for delivering fluid to an inner ear of a subject includes a septum configured to be embedded in the inner ear or on a promontory bone of the subject, a spear connector having a needle for insertion into the septum, a catheter in fluid communication with the spear connector, a fixation device configured to secure the septum to the inner ear or the promontory bone.

Abstract: An implantable drug delivery system includes a middle ear section with a proximal end fixed to a tympanic membrane of a patient, and a distal end that penetrates through a fluid-tight sealed opening into the inner ear. An inner ear section has a proximal end that is connected to the distal end of the middle ear guide member at the sealed opening, and a closed distal end terminating the inner ear holding member some predetermined distance within the cochlea. A hollow interior of the inner ear section is configured for containing a replaceable pharmaceutical agent, and an outer surface is configured to release the pharmaceutical agent from the hollow interior into the inner ear of the patient. The middle ear section and the inner ear section are configured to cooperate for replacing the pharmaceutical agent through the proximal end of the middle ear section to the inner ear section.

Abstract: A fluid delivery system includes an implantable fluid source, a first catheter in fluid communication with the implantable fluid source, and an implantable micro-valve in fluid communication with the first catheter, the micro-valve configured to be located within a round window or to be secured to a promontory bone of a cochlea.

Abstract: An implantable drug delivery system includes a middle ear section with a proximal end fixed to a tympanic membrane of a patient, and a distal end that penetrates through a fluid-tight sealed opening into the inner ear. An inner ear section has a proximal end that is connected to the distal end of the middle ear guide member at the sealed opening, and a closed distal end terminating the inner ear holding member some predetermined distance within the cochlea. A hollow interior of the inner ear section is configured for containing a replaceable pharmaceutical agent, and an outer surface is configured to release the pharmaceutical agent from the hollow interior into the inner ear of the patient. The middle ear section and the inner ear section are configured to cooperate for replacing the pharmaceutical agent through the proximal end of the middle ear section to the inner ear section.

Abstract: An implantable electrode is described for a cochlear implant patient with a malformed common cavity cochlea having a single internal cavity defined by an outer cavity wall or patients having an incomplete partition or conventional spiral-shaped cochlea. An intra-cochlear electrode array is configured to be inserted into the cochlea through a single cochleostomy opening. Outer array branches are closable about a center axis and the electrode array is configured to be closed into a single tube including the array branches for insertion through the single cochleostomy opening into the internal chamber of the cochlea. The electrode array opens within the internal cavity after insertion into the cochlea so that the array branches move away from the center axis to lie with their outer surfaces against the outer cavity wall to deliver the electrical stimulation signals through the stimulation contacts to adjacent neural tissue for auditory perception by the patient.

Abstract: An electrode insertion support device is used for inserting a cochlear implant electrode into a cochlea scala of a patient cochlea. A stiff electrode holder encloses at least a portion of a cochlear implant electrode while allowing the electrode within to slide freely. A pointed distal tip of the electrode holder is adapted to pierce an electrode opening through an outer surface of the patient cochlea into the cochlea scala. The insertion support device prevents an apical tip of the enclosed electrode from contacting tissues around the electrode opening during the insertion surgery.

Abstract: A fluid delivery system includes an implantable fluid source, a first catheter in fluid communication with the implantable fluid source, and an implantable micro-valve in fluid communication with the first catheter, the micro-valve configured to be located within a round window or to be secured to a promontory bone of a cochlea

Abstract: An implant includes a humidity sensor for generating a signal indicative of humidity within the implant. A controller within the implant receives the signal indicative of humidity, and controls the implant based on the signal indicative of humidity.

Abstract: An implant includes a humidity sensor for generating a signal indicative of humidity within the implant. A controller within the implant receives the signal indicative of humidity, and controls the implant based on the signal indicative of humidity.

Abstract: A low-power implant system. The system includes an implant for implantation into a person, such as a cochlear implant or a middle ear implant. The implant is capable of communicating with a device via transmission of ultra wideband pulses. The device may be adapted to be worn external to the person, or may be a second implant. So as to conserve battery power, the transmitted ultra wideband pulses may have a low duty cycle of approximately 1/1000 or less. Power savings may also be realized by using time-gating amplifiers in the implant and/or device receiver.

Abstract: A low-power implant system. The system includes an implant for implantation into a person, such as a cochlear implant or a middle ear implant. The implant is capable of communicating with a device via transmission of ultra wideband pulses. The device may be adapted to be worn external to the person, or may be a second implant. So as to conserve battery power, the transmitted ultra wideband pulses may have a low duty cycle of approximately 1/1000 or less. Power savings may also be realized by using time-gating amplifiers in the implant and/or device receiver.

Abstract: An implantable electronic system is described. An implantable power supply includes multiple power input ports for receiving an externally generated power supply signal, and multiple power output ports for developing a detected power signal. An implantable prosthetic processing module includes multiple prosthetic processing input ports connected by wire to the power output ports for receiving the detected power signal, and multiple prosthetic processing output ports for developing a prosthetic stimulation signal output for electrically stimulating target neural tissue. Each of the multiple ports is adapted to operate without developing a dc potential.

Abstract: An electrode for an implantable prosthesis includes a flexible front end including one or more metal contacts and a back end including one or more metal contacts. The electrode has a cross-sectional shape along the electrode, and the cross-sectional shape has a discontinuity between the flexible front end and the back end. The cross-sectional shape does not have a substantially constant diameter and does not have a continuously growing diameter. The cross-sectional shape of the flexible front end is substantially smaller than the cross-sectional shape of the back end such that forces required to bend the flexible front end are less than forces required to bend the back end.

Abstract: A cochlear implant system is described. An implantable housing includes an electronics module containing circuitry for developing an electrical stimulation signal for the inner ear, and a fluid channel port for receiving therapeutic fluid for the inner ear. An electrode array includes multiple electrode contacts in electrical communication with the electronics module for stimulating neural tissue of the inner ear with the electrical stimulation signal, and a fluid delivery channel for delivering the therapeutic fluid from the fluid channel port to the inner ear.

Abstract: A hearing enhancement includes an audio processor that generates an electrical audio signal and transmits the signal to a coil. The coil is implanted into a patient in a position that results in transmission of mechanical stimulation to the inner ear when the coil is spatially displaced. A permanent magnet is placed in proximity to the coil so that when the coil receives the electrical audio signal form the processor, the induced coil magnetic field in the coil interacts with the magnetic field from the permanent magnet to spatially displace the coil and, as a result, transmit the mechanical stimulation to the inner ear.

Abstract: An implantable device and corresponding method for suppression of tinnitus are described. An implantable signal processing module develops a stimulation signal for application to audio sensing tissue of the user. The signal processing module includes a tinnitus suppression mode in which the stimulation signal is unrelated to environmental sound near the user.