First & Ten, Inc.
Country not established
- Devices
- 1
What First & Ten, Inc. makes
First & Ten, Inc. manufactures THE VERSA-BED, a Class I medical device designed for patient positioning and mobility support in clinical settings.
THE VERSA-BED is regulated under 510(k) clearance by the FDA and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
The Versa-Bed Ref K792298
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does First & Ten, Inc. have in the registry?
The registry currently lists 1 device for First & Ten, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list First & Ten, Inc.'s devices?
Among its 1 most recently registered device, First & Ten, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do First & Ten, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for First & Ten, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from First & Ten, Inc. in the registry?
The most recently registered devices listed for First & Ten, Inc. include THE VERSA-BED.