Neurelec
Country not established
Neurelec is a medical device manufacturer, with 58 devices listed in FDA GUDID (FDA Class III, I and II) as of 13 Nov 2026.
- Devices
- 58
Registry facts
- Registries
- FDA GUDID 58
- Device classes
- FDA Class III 52
- FDA Class I 5
- FDA Class II 1
- Identifiers
- DUNS 285420530
What Neurelec makes
The company designs and manufactures cochlear implant systems, including auditory brainstem implants and sound processors, as well as programming interfaces for hearing aid and implant systems. These devices are intended for individuals with severe to profound hearing loss, providing auditory stimulation through direct electrical stimulation of the auditory nerve or cochlear nerve.
The portfolio includes devices classified as Class I, Class II, and Class III under regulatory frameworks, with products listed in the FDA’s Unique Device Identifier (UDI) database. The company operates primarily in the United States, adhering to domestic regulatory requirements for medical devices.
Catalogue
Search and filter all 58 devicesShowing 1-50 of 58
Company details
- DUNS number
- 285420530
- Phone
- 1-888-277-8121
Frequently asked questions
How many devices does NEURELEC have in the registry?
The registry currently lists 58 devices for NEURELEC. Devices recorded under merged duplicate company entries are counted once.
Which registries list NEURELEC's devices?
Among its 50 most recently registered devices, NEURELEC has devices listed in FDA GUDID (50 devices).
What risk classes do NEURELEC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for NEURELEC's devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from NEURELEC in the registry?
The most recently registered devices listed for NEURELEC include Neuro Cochlear Implant System M80181, Neuro Cochlear Implant System 158031, Neuro Cochlear Implant System M80184 and Neuro Cochlear Implant System M80175.