Tenstaple, Inc.
Country not established
- Devices
- 1
What Tenstaple, Inc. makes
Tenstaple, Inc. manufactures the Tenstaple Orthopedic Stapling System, a Class II medical device used for orthopedic stapling procedures.
The device is regulated under the FDA 510(k) pathway and is listed in the FDA 510(k) registry. Tenstaple, Inc. is based in the United States.
Catalogue
Tenstaple Orthopedic Stapling System Ref K896471
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tenstaple, Inc. have in the registry?
The registry currently lists 1 device for Tenstaple, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tenstaple, Inc.'s devices?
Among its 1 most recently registered device, Tenstaple, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Tenstaple, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tenstaple, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tenstaple, Inc. in the registry?
The most recently registered devices listed for Tenstaple, Inc. include TENSTAPLE ORTHOPEDIC STAPLING SYSTEM.