Dentron, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dentron-Exact - Tray Ref K820997
Regimes: 510(k) Registry: 510(k)Dentron-Direct-Tray Ref K820998
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dentron, Inc. have in the registry?
The registry currently lists 2 devices for Dentron, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dentron, Inc.'s devices?
Among its 2 most recently registered devices, Dentron, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dentron, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dentron, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dentron, Inc. in the registry?
The most recently registered devices listed for Dentron, Inc. include DENTRON-EXACT - TRAY and DENTRON-DIRECT-TRAY.