Osseous Technologies of America
Country not established
- Devices
- 1
What Osseous Technologies of America makes
Osseous Technologies of America manufactures collagen-based biomaterials designed for bone regeneration and tissue integration in surgical applications.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) pathway. The portfolio is listed in the FDA’s 510(k) registry.
Catalogue
Ota Collagen Biomaterial Ref K073685
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osseous Technologies of America have in the registry?
The registry currently lists 1 device for Osseous Technologies of America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osseous Technologies of America's devices?
Among its 1 most recently registered device, Osseous Technologies of America has devices listed in FDA 510(k) (1 device).
What risk classes do Osseous Technologies of America's devices fall under?
Among its 1 most recently registered device, the classes recorded for Osseous Technologies of America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osseous Technologies of America in the registry?
The most recently registered devices listed for Osseous Technologies of America include OTA COLLAGEN BIOMATERIAL.