Berni Farns Incorporated
Country not established
- Devices
- 1
What Berni Farns Incorporated makes
Berni Farns Incorporated manufactures the BONETRAP, a medical device designed for orthopedic applications, likely intended for the fixation or stabilization of bone fragments during surgical procedures.
The BONETRAP is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Bonetrap Ref K120189
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Berni Farns Incorporated have in the registry?
The registry currently lists 1 device for Berni Farns Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Berni Farns Incorporated's devices?
Among its 1 most recently registered device, Berni Farns Incorporated has devices listed in FDA 510(k) (1 device).
What risk classes do Berni Farns Incorporated's devices fall under?
Among its 1 most recently registered device, the classes recorded for Berni Farns Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Berni Farns Incorporated in the registry?
The most recently registered devices listed for Berni Farns Incorporated include BONETRAP.