Audio-Aid, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Audio-Aid, Inc. makes
Audio-Aid, Inc. makes hearing aids, including the AUDIO-ADI, AA series and in-the-ear hearing aids RX10 and RX20.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Audio-Adi, Aa Series Ref K820993
510(k) 510(k)In-The-Ear Hearing Aid RX10 & 20 Ref K840891
510(k) 510(k)
Frequently asked questions
How many devices does Audio-Aid, Inc. have in the registry?
The registry currently lists 2 devices for Audio-Aid, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Audio-Aid, Inc.'s devices?
Among its 2 most recently registered devices, Audio-Aid, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Audio-Aid, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Audio-Aid, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Audio-Aid, Inc. in the registry?
The most recently registered devices listed for Audio-Aid, Inc. include AUDIO-ADI, AA SERIES and IN-THE-EAR HEARING AID RX10 & 20.