A middle ear implant system includes a bone conduction transducer configured for fixed attachment to skull bone of a patient beneath the skin behind the ear, and for generating sound vibrations from an external communications signal received through the skin for coupling to the skull bone for bone conduction sound perception by the patient. A malleable ossicle connector is connected to the bone conduction transducer and a middle ear hearing structure of the patient. And one or more isolation springs are configured for placement at the fixed attachment of the bone conduction transducer to the skull bone to acoustically decouple the bone conduction transducer from the skull bone to avoid bone conduction sound perception so that sound perception from the external communications signal is solely via the middle ear sound perception from vibrations coupled to the middle ear hearing structure by the ossicle connector.

Systems and methods for detecting when a device is placed into an operational position are disclosed. Upon determination that the device is in the operational position, one or more processes can be executed. Execution or initialization of the processes upon detection of the operational position provides for the determination of optimal settings than would otherwise be determined if the processes automatically executed before detection of the operational position. Further aspects of the present disclosure relate to determining when the device is no longer in an operational position upon which time the execution of the processes are terminated. The settings in place upon termination can be saved and reapplied the next time the device is in the operational position.

The present invention relates to a hearing aid (1) which is inserted to body by surgery in order to enable patients with very advanced and total sensorineural hearing loss to detect sounds, stimulate cochlea or any point on the auditory pathway electrically according to the audio information received from external environment, can also be used without its external part, and parts of which can be replaced without being completely removed from the body in case of a malfunction.

The invention relates to an irradiation apparatus for the prophylaxis of hearing impairment and/or vertigo, to a system of functionally connected apparatus components which interact with each other, and a method that uses the irradiation apparatus for the prophylactic irradiation of the inner ear with photons in order to prevent hearing impairment and/or vertigo in a wearer of the irradiation apparatus.

A percutaneous bone conduction auditory prosthesis utilizes a multipole magnetic coupling system to secure the external device to an abutment that is secured to the skull of a recipient. With the multipole magnetic coupling system, a very strong retention force is formed between the device and the abutment. The multipole magnetic coupling system can include a complex array of exposed poles, such that the retention forces are coordinated with a mating abutment.

An external processor device for a hearing implant system is described. An audio signal processor is coupled to an audio input providing an electrical audio input signal and develops a corresponding implant stimulation signal output. A stimulation signal transmitter is coupled to the signal processor and receives the implant stimulation signal for transmission to an implanted portion of the hearing implant system. The device includes an audio bypass mode which provides the audio input signal to the stimulation signal transmitter for transmission.

Methods and apparatus for transmitting vibrations via an electronic and/or transducer assembly through a tooth or teeth are disclosed herein. The assembly may be attached, adhered, or otherwise embedded into or upon a removable oral appliance to form a hearing aid assembly. Such an oral appliance may be a custom-made device. The electronic and transducer assembly may receive incoming sounds either directly or through a receiver to process and amplify the signals and transmit the processed sounds via a vibrating transducer element coupled to a tooth or other bone structure, such as the maxillary, mandibular, or palatine bone structure.

An exemplary system includes an electro-acoustic stimulation (EAS) sound processor, a cochlear implant communicatively coupled to the EAS sound processor, an electrode array communicatively coupled to the cochlear implant, and a receiver communicatively coupled to the EAS sound processor and configured to be in communication with an ear of a patient. The EAS sound processor 1) directs, while in a self-fitting mode, the receiver to apply acoustic stimulation to the patient, 2) records, using at least one electrode included in the electrode array, an evoked response that occurs in response to the acoustic stimulation, 3) compares the evoked response to a baseline evoked response recorded by the EAS sound processor prior to recording the evoked response, and 4) performs a predetermined action based on the comparison between the evoked response and the baseline evoked response. Corresponding systems and methods are also disclosed.

A bilateral hearing implant system has a left side and a right side. Left and right side filter bank pre-processors preprocess left and right microphone signals to generate band pass signals for each side. A bilateral signal processing arrangement processes the band pass signals in a time sequence of stimulation frames. The signal processing module includes a bilateral channel selection module synchronously selects for each stimulation frame a set of stimulation channels for each side based on spectral content of the band pass signals. Left and right side signal processing submodules process for each stimulation frame a limited subset of each side band pass signals corresponding to the selected stimulation channels to generate electrical stimulation signals.

A malleable implantable medical device for implanting in a recipient comprising a flexible region of the medical device, one or more structures proximate to the flexible region, wherein the one or more structures is configured to provide a bending force to the flexible region, and one or more hermetically sealed medical components coupled to the flexible region, wherein the one or more medical components is configured to provide a therapeutic effect on the recipient.