Gn Danavox, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Danavox Models 163/162 Bte Ref K971032
Regimes: 510(k) Registry: 510(k)Audallion Iii Hearing System Ref K971031
Regimes: 510(k) Registry: 510(k)143 Series Bte Ref K905692
Regimes: 510(k) Registry: 510(k)Danavox Model Cic Ref K942331
Regimes: 510(k) Registry: 510(k)Custom In-The-Ear Ref K863975
Regimes: 510(k) Registry: 510(k)Dfs Genius Bte Ref K924185
Regimes: 510(k) Registry: 510(k)133 Series Bte Ref K905679
Regimes: 510(k) Registry: 510(k)Discretion, In The Canal Hearing Instrument Ref K896995
Regimes: 510(k) Registry: 510(k)Cerumen Filter Ref K891594
Regimes: 510(k) Registry: 510(k)Cas (Computerized Analyzer System) Ref K896996
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gn Danavox, Inc. have in the registry?
The registry currently lists 10 devices for Gn Danavox, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gn Danavox, Inc.'s devices?
Among its 10 most recently registered devices, Gn Danavox, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Gn Danavox, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Gn Danavox, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gn Danavox, Inc. in the registry?
The most recently registered devices listed for Gn Danavox, Inc. include DANAVOX MODELS 163/162 BTE, AUDALLION III HEARING SYSTEM, 143 SERIES BTE and DANAVOX MODEL CIC.