Audifon-USA, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
- 510(k) 510(k)
An Evo 1, Cs Evo 1, Contact Mini, Apollon Ref K121793
510(k) 510(k)
Frequently asked questions
How many devices does Audifon-USA, Inc. have in the registry?
The registry currently lists 4 devices for Audifon-USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Audifon-USA, Inc.'s devices?
Among its 4 most recently registered devices, Audifon-USA, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Audifon-USA, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Audifon-USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Audifon-USA, Inc. in the registry?
The most recently registered devices listed for Audifon-USA, Inc. include AUDIFON ARRIVA CIC, IS, IS+, M, S, S+, X TRT, AUDIFON VICO, AUDIFON PRADO, AUDIFON ELIA, CIC, IS, IS+, M, S TRT, JUMP S+ TRT, JUMP CIC TRT, JUMP S TRT, JUMP C TRT, AUDIFON SUENO CIC, AUDIFON SUENO S, AUDIFON SUENO T CIC, AUDIFON SUENO T S and AN EVO 1, CS EVO 1, CONTACT MINI, APOLLON.