Tri-Stage, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Tri-Stage, Inc. makes
Tri-Stage, Inc. manufactures dental burs for cutting and shaping teeth, the TS-I dental implant for osseointegrated tooth replacement, and tissue punches for precise biopsy or surgical sampling in oral and maxillofacial procedures.
The company’s portfolio includes Class I and Class II devices, with submissions recorded in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Dental Burs Ref K882183
Regimes: 510(k) Registry: 510(k)Tri-Stage (Ts-I) Dental Implant Ref K880220
Regimes: 510(k) Registry: 510(k)Tissue Punch Ref K882834
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tri-Stage, Inc. have in the registry?
The registry currently lists 3 devices for Tri-Stage, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tri-Stage, Inc.'s devices?
Among its 3 most recently registered devices, Tri-Stage, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Tri-Stage, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Tri-Stage, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tri-Stage, Inc. in the registry?
The most recently registered devices listed for Tri-Stage, Inc. include DENTAL BURS, TRI-STAGE (TS-I) DENTAL IMPLANT and TISSUE PUNCH.