Orthonetx, Inc.
Country not established
- Devices
- 1
What Orthonetx, Inc. makes
Orthonetx, Inc. manufactures the Generos SB Small Bone Distraction Implant, a device designed for small bone lengthening procedures.
The implant is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Generos Sb Small Bone Distraction Implant Ref K051162
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthonetx, Inc. have in the registry?
The registry currently lists 1 device for Orthonetx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthonetx, Inc.'s devices?
Among its 1 most recently registered device, Orthonetx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Orthonetx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orthonetx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthonetx, Inc. in the registry?
The most recently registered devices listed for Orthonetx, Inc. include GENEROS SB SMALL BONE DISTRACTION IMPLANT.