Ardent Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Articulating Paper Ref K832647
Regimes: 510(k) Registry: 510(k)Exacta-Film Ref K842512
Regimes: 510(k) Registry: 510(k)Siliva Ejector/Oral Cavity Evacuator Ref K864300
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ardent Intl., Inc. have in the registry?
The registry currently lists 3 devices for Ardent Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ardent Intl., Inc.'s devices?
Among its 3 most recently registered devices, Ardent Intl., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ardent Intl., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ardent Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ardent Intl., Inc. in the registry?
The most recently registered devices listed for Ardent Intl., Inc. include ARTICULATING PAPER, EXACTA-FILM and SILIVA EJECTOR/ORAL CAVITY EVACUATOR.