Audiofon USA, Inc.
Country not established
- Devices
- 1
What Audiofon USA, Inc. makes
Audiofon USA, Inc. manufactures the audifon Tinnitus-Module, a device designed to manage and alleviate symptoms of tinnitus through auditory stimulation.
The audifon Tinnitus-Module is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
audifon Tinnitus-Module Ref K171243
510(k) 510(k)
Frequently asked questions
How many devices does Audiofon USA, Inc. have in the registry?
The registry currently lists 1 device for Audiofon USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Audiofon USA, Inc.'s devices?
Among its 1 most recently registered device, Audiofon USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Audiofon USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Audiofon USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Audiofon USA, Inc. in the registry?
The most recently registered devices listed for Audiofon USA, Inc. include audifon Tinnitus-Module.