Endodent, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Endodent, Inc. makes
Endodent, Inc. manufactures endodontic materials and instruments, including paper points for root canal treatment, gutta-percha filling material, and gutta-percha points used in dental procedures to seal treated root canals.
These products are classified under FDA Class I and Class U devices and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Point, Paper Endodontic Ref K830814
Regimes: 510(k) Registry: 510(k)Gutta Percha Ref K863411
Regimes: 510(k) Registry: 510(k)Gutta Percha Points Ref K863638
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endodent, Inc. have in the registry?
The registry currently lists 3 devices for Endodent, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endodent, Inc.'s devices?
Among its 3 most recently registered devices, Endodent, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Endodent, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Endodent, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Endodent, Inc. in the registry?
The most recently registered devices listed for Endodent, Inc. include POINT, PAPER ENDODONTIC, GUTTA PERCHA and GUTTA PERCHA POINTS.