Agnovos Healthcare Usa, LLC
Country not established FDA establishment FEI 3011662387
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
What Agnovos Healthcare Usa, LLC makes
AGNOVOS Healthcare USA, LLC manufactures the JGH1 Bone Graft Substitute, a bone graft material, and the JGH1 Core Decompression Procedure Kit, a kit for performing core decompression procedures.
Both devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
JGH1 Bone Graft Substitute Ref K181342
510(k) 510(k)JGH1 Core Deccompression Procedure Kit Ref K181585
510(k) 510(k)
Company details
- FDA FEI number
- 3011662387
- Address
- 7301 CALHOUN PL STE 100, Rockville, MD, 20855
Frequently asked questions
How many devices does AGNOVOS HEALTHCARE USA, LLC have in the registry?
The registry currently lists 2 devices for AGNOVOS HEALTHCARE USA, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list AGNOVOS HEALTHCARE USA, LLC's devices?
Among its 2 most recently registered devices, AGNOVOS HEALTHCARE USA, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do AGNOVOS HEALTHCARE USA, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for AGNOVOS HEALTHCARE USA, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from AGNOVOS HEALTHCARE USA, LLC in the registry?
The most recently registered devices listed for AGNOVOS HEALTHCARE USA, LLC include JGH1 Bone Graft Substitute and JGH1 Core Deccompression Procedure Kit.