Tri-State
Country not established
- Devices
- 1
What Tri-State makes
Tri-State manufactures the Centurion Skin Staple Remover, a device designed for the removal of surgical staples from skin incisions in clinical settings.
The Centurion Skin Staple Remover is classified as a Class I medical device and is listed under FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Centurion Skin Staple Remover Ref K822365
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tri-State have in the registry?
The registry currently lists 1 device for Tri-State. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tri-State's devices?
Among its 1 most recently registered device, Tri-State has devices listed in FDA 510(k) (1 device).
What risk classes do Tri-State's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tri-State's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tri-State in the registry?
The most recently registered devices listed for Tri-State include CENTURION SKIN STAPLE REMOVER.