Biomet Osteobiologics
Country not established
- Devices
- 1
What Biomet Osteobiologics makes
Biomet Osteobiologics makes bone void fillers, specifically the BONEPLAST QS calcium sulfate bone void filler, which is a synthetic material used to fill bony defects or gaps in the skeletal system.
The BONEPLAST QS device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Boneplast Qs Calcium Sulfate Bone Void Filler Ref K070864
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomet Osteobiologics have in the registry?
The registry currently lists 1 device for Biomet Osteobiologics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomet Osteobiologics's devices?
Among its 1 most recently registered device, Biomet Osteobiologics has devices listed in FDA 510(k) (1 device).
What risk classes do Biomet Osteobiologics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Biomet Osteobiologics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biomet Osteobiologics in the registry?
The most recently registered devices listed for Biomet Osteobiologics include BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER.