Ortheon Medical, LLC
Country not established
- Devices
- 1
What Ortheon Medical, LLC makes
Ortheon Medical, LLC manufactures the TENO FIX, a device designed for orthopedic fixation applications, likely used in bone stabilization or fracture treatment.
The TENO FIX is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Teno Fix Ref K023594
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ortheon Medical, LLC have in the registry?
The registry currently lists 1 device for Ortheon Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ortheon Medical, LLC's devices?
Among its 1 most recently registered device, Ortheon Medical, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Ortheon Medical, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ortheon Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ortheon Medical, LLC in the registry?
The most recently registered devices listed for Ortheon Medical, LLC include TENO FIX.