Abstract: A totally implantable cochlear implant system forming a single implantable unit (40). The unit (40) has an implantable power source (43) that provides the power requirements of the implantable unit (40). The unit (40) also has an on board microphone (42) that detects external sounds, such as speech, and outputs acoustic signals representative of the detected sounds. The unit further includes speech processor circuitry (44) that directly receives the acoustic signals from the microphone (42) and converts the signals into stimulation signals representative of the detected sounds. An electrode array (20) suitable for insertion of the cochlea (42) of an implantee receives the stimulation signals and transmits electrical stimulations to the implantee's auditory nerve (9).

Abstract: The present application discloses systems and methods for performing a weighting operation in a stimulation module of a stimulation prosthesis. Accordingly, a command module transmits one data word (i.e., the channel and amplitude value) to the stimulation module. The stimulation module then determines the individual electrodes and magnitudes of electrical signals to apply thereto so as to achieve appropriate stimulation on the channel. In accordance with one embodiment, a stimulation module includes a receiver that is configured for receiving stimulation data transmitted by the command module, the stimulation data defining a channel and an amplitude, a weighting unit configured for calculating, based on the channel and amplitude value, a set of magnitudes, and an arrangement of current sources-and-switches configured for applying current to the array of electrodes based on the calculated set of magnitudes.

Abstract: The present invention provides for fitting a multimodal hearing system to a recipient. Such fitting may include determining a desired perception for an input signal, receiving a measurement of a perception evoked by applying to the recipient one or more stimulation signals that correspond to the input signal, wherein the one or more stimulation signals applied using two or more stimulation modes, and each stimulation signal is determined using stimulus mode weighting, and adjusting one or more of the stimulus mode weightings based on the difference between the measured evoked perception and the desired perception. A multimodal hearing system is able to stimulate using an acoustic, electrical, mechanical mode and/or photo effect mode.

Abstract: A housing for an implantable device for mounting to a patient's bone is disclosed. The housing comprises one or more surfaces, wherein at least one of the surfaces is substantially orthogonal to an implant axis and is configured to abut the patient's bone, and a first osseointegrating protuberance extending from one of the surfaces, wherein a longitudinal axis of the first protuberance is disposed at an acute first angle relative to the implant axis.

Abstract: The measurement of recipient-specific operating parameters for each of a plurality of stimulation channels of a stimulating medical device. Generally, a recipient-specific operating parameter is measured for selected stimulation channels. These measured values are then used to estimate the same operating parameter for the remaining stimulation channels. For each such remaining stimulation channel, the accuracy of the estimated operating parameter value is determined, resulting in the estimated operating parameter value being deemed either valid or invalid. The validated values are retained while in invalidated values are replaced with a directly-measured or re-estimated operating parameter value.

Abstract: A method for generating a new set of MRI images of a region of a recipient in which an implanted medical device having magnetic properties is located. The method includes scanning a plurality of scan slices of the recipient with an MRI machine set at a first fat shift direction to generate a first set of MRI images and rescanning the plurality of scan slices with a fat shift direction different than the first fat shift direction to obtain a second set of MRI images. At least one of the MRI images of the first set and the second set including an artifact resulting from the implanted medical device. The method further includes comparing respective artifacts of the MRI images of the first and second sets, and selecting one of the compared MRI images based on the distortion to the respective MRI image created by the respective artifact.

Abstract: Disclosed herein are medical prostheses including a cochlear implant that includes circuitry enclosed within a housing and at least one electrode lead extending from the housing. The electrode lead comprises a conducting pathway and an electrode terminal at one end of the electrode lead. The conducting pathway connects the circuitry with the electrode terminal, and insulation (or an insulating sleeve) encloses at least a portion of the conducting pathway. In some embodiments, the electrode terminal has a lower thermal conductivity relative to the implant housing. In further embodiments, the insulation has thermal conductivity and thermal conduction properties that cause at least some thermal energy in the conducting pathway to flow into the insulation rather than to the electrode terminal. In still further embodiments, at least one of the electrode terminal or the electrode lead includes at least one thermal mass enhancing structure.

Abstract: A bone conduction device configured to couple to an abutment of an anchor system anchored to a recipient's skull. The bone conduction device includes a vibrating electromagnetic actuator configured to vibrate in response to sound signals received by the bone conduction device, and a coupling apparatus configured to attach the bone conduction device to the abutment so as to impart to the recipient's skull vibrations generated by the vibrating electromagnetic actuator. The vibrating electromagnetic actuator includes a bobbin assembly and a counterweight assembly. Two axial air gaps are located between the bobbin assembly and the counterweight assembly and two radial air gaps are located between the bobbin assembly and the counterweight assembly. No substantial amount of the dynamic magnetic flux passes through the radial air gaps.

Abstract: Disclosed herein are medical prostheses including a cochlear implant that includes circuitry enclosed within a housing and at least one electrode lead extending from the housing. The electrode lead comprises a conducting pathway and an electrode terminal at one end of the electrode lead. The conducting pathway connects the circuitry with the electrode terminal, and insulation (or an insulating sleeve) encloses at least a portion of the conducting pathway. In some embodiments, the electrode terminal has a lower thermal conductivity relative to the implant housing. In further embodiments, the insulation has thermal conductivity and thermal conduction properties that cause at least some thermal energy in the conducting pathway to flow into the insulation rather than to the electrode terminal. In still further embodiments, at least one of the electrode terminal or the electrode lead includes at least one thermal mass enhancing structure.

Abstract: A method of forming a braze join between two components is disclosed, in which braze material is introduced into a gap between the two components by capillary action. This assists in reducing flooding. Also disclosed is a component for use with the method, and an assembly produced by the method. In one form, the component comprises a recess or reservoir for storing braze material, in fluid communication with an aperture to allow the braze material to be drawn into the gap by capillary forces. The method may be used in a number of applications including medical devices and more specifically, a cochlear implant.

Abstract: An hearing prosthesis configured to cancel received bone-conducted sound. The hearing prosthesis comprises: first and second matched microphones configured to be implanted in a recipient in a spaced arrangement such that the first microphone receives air-conducted sound signals and bone-conducted sound signals substantially simultaneously, and wherein the second microphone receives bone-conducted sound signals at substantially the same time as the first microphone and receives the air-conducted sound signals after a time delay. The time delay results in a relative phase difference between the air-conducted sound signals and the bone-conducted sound signals received by the second microphone. The prosthesis also comprises a noise cancellation system configured to cancel, based on the phase difference, the bone-conducted sound signals received by the first and second microphones.

Abstract: An implantable hearing unit is provided that includes an implantable microphone, a rechargeable power storage device and a speech signal processor. The hearing unit further includes a signal coupling device that is adapted for electrical interconnection to an implantable auditory stimulation device, which is operative to stimulate an auditory component of a patient. Such a stimulation device may include cochlear implants, brain stem stimulation systems, auditory nerve stimulation systems, and middle or inner ear transducer systems. The signal coupling device is operative to provide processed drive signals from the signal processor to the stimulation device as well provide power from the power storage device to operate the stimulation device. In one arrangement, the signal coupling device is a wireless coupling between first and second coils. In such an arrangement, the hearing unit may be utilized with an existing implanted stimulation device to make that device a fully implanted hearing system.

Abstract: Coating an elongate, uncoated conductive element with a barrier layer to form an insulated conductive element. The insulated conductive element comprises substantially continuously coated elongate sections separated by uncoated gaps which are substantially small relative to the lengths of the coated sections.

Abstract: A bone conduction device including a coupling configurable to form a coupling with a bone, a transducer module configurable to vibrate in accordance with one or more operational characteristics of the device; and a sensor module configurable to adjust the one or more operational characteristics in response to one or more of a reorientation of a portion of the device and a movement of the portion relative to the coupling.

Abstract: The present application discloses a vibration-based hearing prosthesis configured to measure the vibration applied by a hearing prosthesis to the skull of the hearing prosthesis recipient while the recipient is wearing the hearing prosthesis. Directly measuring the applied vibration in situ allows hearing characteristics to be more accurately mapped to voltage inputs. A recipient's hearing threshold and associated voltage input may be directly measured. Additionally, measuring the applied vibrations allows co-listening. A doctor can monitor the sound output from a vibration-based hearing prosthesis as it is worn by a recipient. Directly measuring the vibration output also allows an additional degree of freedom in diagnostics because a recipient can perform diagnostic tests at home.

Abstract: An implantable medical device comprising first and second coils each comprising one or more circular windings defining a diameter. Each of the first and second coils have a length, wherein the diameter of the one or more windings of the first coil are greater than the length of the first coil, and wherein the diameter of the one or more windings of the second coil are smaller than the length of the second coil, and wherein at least one of the one or more windings of the first coil is substantially orthogonal to at least one of the windings of the second coil.

Abstract: An implantable apparatus, such as a cochlear implant, for delivering electrical plasticity informative stimuli to a neural network of an implantee. The apparatus comprises a stimulator device (40) that generates stimulation signals, and an electrode array (20) that receives the stimulation signals and delivers the stimuli to the neural network of the implantee in response to the signals. The stimuli delivered to the implantee facilitates and/or controls the production and/or release of naturally occurring agents into the neural network to influence the functionality thereof.

Abstract: Methods and systems are provided for determining whether signals to be applied by a bone conduction device would be masked by signals arriving at the good ear of a single sided deaf patient. The bone conduction device then applies stimulation for frequency components of the sound received by the bone conduction device that would not be masked by sound received by the patient's good ear. In applying the stimulation, the bone conduction device may apply a gain to compensate for the head shadow effect. This gain may be determined by inverting at least a portion of a curve for the head shadow effect.

Abstract: A bone conduction device for enhancing the hearing of a recipient, comprising: a sound input element configured to receive an acoustic sound signal; an electronics module configured generate an electrical signal representing the acoustic sound signal; a transducer configured to generate mechanical forces representing the electrical signal for delivery to the recipient's bone; and one or more vibration extensions mechanically coupled to the transducer and configured to be inserted into the ear canal of the recipient, and further configured to vibrate in order to transmit the mechanical forces generated from the transducer to the recipient's bone.

Abstract: A bone conduction device, comprising: a sound input element configured to receive an acoustic sound signal; an electronics module configured generate an electrical signal representing said acoustic sound signal; and a transducer configured to generate motion of a mass component based on said electrical signal so as to generate one or more mechanical forces resulting in one or more of motion and vibration of a recipient's skull thereby causing sound perception, wherein one or more of the size and shape of said mass component is selectable at least partially based on a desired mechanical force to be generated by said transducer.