Abstract: A hearing aid module (60) is shaped for insertion into a tunnel (40) made through the soft tissue that connects the retro-auricular space (50) with the ear canal (30). A hollow tube (44) may first be chronically or acutely implanted in such tunnel, and the hearing aid module inserted into the tube. The tube or hearing aid module may have a coating (45) containing a steroid or drug adapted to minimize infection and/or inflammation. The hearing aid module contains a speaker (65), a battery or other power source (66) powering the module, signal processing circuitry (67), and a microphone (63). Telemetry circuitry (69) within the module allows the signal processing circuitry to be programmed with a desired frequency response or signal processing strategy using an external programming unit (74). A remote control unit (75) permits the user to make simple adjustments, such as volume and/or tone control.

Abstract: A personal sound link module (60) is inserted into a tunnel (40) made through the soft tissue connecting the retro-auricular space (50) with the ear canal (30). The module contains an acoustic transducer (65), located at the distal part (68) of the module, close to or inside the ear canal, an antenna (64) that receives and also potentially sends signals to a remote source, signal processing circuitry (67), telemetry circuitry (69), a power source (66) that powers the module, and possibly a microphone (63). Signals transmitted from a remote source are received through the antenna and telemetry circuitry, processed, and presented to the acoustic transducer, where they are converted to sound waves broadcast into the user's ear canal. The remote source may be a radio station, radio receiver, CD player, DVD player, tape player, audio system, telephone, TV receiver or station, or other source of audio signals intended to be heard privately by the user.

Abstract: An improved method for securing an external device of a implantable system, in cooperation with an implantable device of the implantable system, uses a medical-pressure-sensitive adhesive pad to attach the external device to skin. Both power and control signals may be transmitted transcutaneously from the external device to the implantable device. Efficient transmission of these signals requires that the external device be securely held in cooperation with the implantable device. The medical-pressure-sensitive adhesive pad acts as an interposing adhesive between the external device and the skin. One side of the pad provides adhesion to the back of the external device. The opposite side of the pad provides adhesion to the skin/hair. The pad includes a tab for easy removal of the pad from the external device. The adhesives have aggressive adhesion to the pad, so that upon the removal of the pad from the skin, and then the external device, all of the adhesive remains on the pad.

Abstract: The invention is a method for increasing the airflow to a zinc-air battery such that the energy density is 500 mwh/cc to 1000 mwh/cc. This allows 8 to 16 hours use as a primary (throw-away) battery, with, for example, high-duty cycle, high-drain cochlear implants, and neuromuscular stimulators for nerves, muscles, and both nerves and muscles together. The systems incorporating the high energy density source are also part of the invention, as well as the resulting apparatus of the method. The uses of this inexpensive, i.e., a $1.00 per day, throw-away primary battery are new uses of the modified zinc-air battery and are directed toward helping people hear again, walk again, and regain body functionality which they have otherwise lost permanently.

Abstract: A myogenic-based evoked response (termed the “MER” for purposes of this application), heretofore considered an undesirable artifact in response to an applied Cochlear stimulus, is deliberately sensed and measured with permanently implanted electrodes connected to a Cochlear implant device. The measured MER is then used to assist in the objective programming of the Cochlear implant. The MER may be measured between two intra-Cochlear electrodes, between one intra-Cochlear electrode and one extra-Cochlear reference electrode, or between two extra-Cochlear electrodes. Because the measured MER is believed to pre-empt the actual stapedius reflex, the electrodes need not be placed into or in close proximity to the stapedial tendon, the stapes, or the facial nerve.

Abstract: The invention is a method for increasing the airflow to a Zinc-air battery such that the energy density is 500 mwh/cc to 1000 mwh/cc. This allows 8 to 16 hours use as a primary (throw-away) battery, with, for example, high-duty cycle, high-drain cochlear implants, and neuromuscular stimulators for nerves, muscles, and both nerves and muscles together. The systems incorporating the high energy density source are also part of the invention, as well as the resulting apparatus of the method. The uses of this inexpensive, i.e., a $1.00 per day, throw-away primary battery are new uses of the modified zinc-air battery and are directed toward helping people hear again, walk again, and regain body functionality which they have otherwise lost permanently.

Abstract: An implantable electrode array, adapted for insertion into a cochlea, provides a multiplicity of exposed electrode contacts, each having a shape, geometry, or makeup that aids in controlling the current flow and current density associated with the electrode contact as a function of position on the electrode contact. In one embodiment, the shape or geometry of the exposed electrode contact controls the contact surface of the electrode contact in a way that varies the current flow and current density as a function of surface area position on the electrode, thereby focusing most of the current to flow through the center of the electrode contact. In another embodiment, the electrode contact is coated with a dielectric or other material that controls the surface contact impedance as a function of distance from the center of the electrode, again focusing most of the current flow through the center of the electrode contact.

Abstract: A cochlear stimulation system includes a speech processing strategy that applies non-auditory-informative stimuli as well as auditory-informative stimuli to the same or neighboring sets of electrodes. The non-auditory-informative stimuli are applied to the auditory neural system for the purpose of influencing the properties and response characteristics of the auditory system so that when the auditory-informative stimuli are applied, such stimuli are more effective at evoking a desired auditory response, i.e., are more effective at allowing the patient to perceive sound. The information-carrying stimuli may be applied to the auditory neural system at the same time as is the non-auditory-informative stimuli, or may be applied during time slots between application of the non-auditory-informative stimuli.