Osstem Germany GmbH
Country not established
- Devices
- 1
What Osstem Germany GmbH makes
Osstem Germany GmbH makes bone graft materials including SUFLEX PUTTY, SUFLEX HEAVY, SUFLEX MONO, and SUFLEX LIGHT.
These devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osstem Germany GmbH have in the registry?
The registry currently lists 1 device for Osstem Germany GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osstem Germany GmbH's devices?
Among its 1 most recently registered device, Osstem Germany GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Osstem Germany GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Osstem Germany GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osstem Germany GmbH in the registry?
The most recently registered devices listed for Osstem Germany GmbH include SUFLEX PUTTY, SUFLEX HEAVY, SUFLEX MONO, SUFLEX LIGHT.