Med-El Corp.
Country not established
- Devices
- 1
What Med-El Corp. makes
Med-El Corp. manufactures the Combi 40+ Cochlear Implant System, a device designed for individuals with severe to profound sensorineural hearing loss who derive insufficient benefit from hearing aids. This system includes an external sound processor and an internal implant that stimulates the auditory nerve, enabling hearing perception.
The Combi 40+ Cochlear Implant System is classified as a Class III medical device under FDA regulations and is authorised via a Premarket Approval (PMA) application. The company is based in the United States.
Catalogue
Combi 40+ Cochlear Implant System Ref P000025
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Med-El Corp. have in the registry?
The registry currently lists 1 device for Med-El Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med-El Corp.'s devices?
Among its 1 most recently registered device, Med-El Corp. has devices listed in FDA PMA (1 device).
What risk classes do Med-El Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Med-El Corp.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Med-El Corp. in the registry?
The most recently registered devices listed for Med-El Corp. include Combi 40+ Cochlear Implant System.