Haider Biologics, LLC
Country not established
- Devices
- 1
What Haider Biologics, LLC makes
Haider Biologics, LLC manufactures the Sorrento Bone Graft Substitute, a product designed to replace or augment bone tissue in surgical procedures.
The Sorrento Bone Graft Substitute is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Sorrento Bone Graft Substitute Ref K141429
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Haider Biologics, LLC have in the registry?
The registry currently lists 1 device for Haider Biologics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Haider Biologics, LLC's devices?
Among its 1 most recently registered device, Haider Biologics, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Haider Biologics, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Haider Biologics, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Haider Biologics, LLC in the registry?
The most recently registered devices listed for Haider Biologics, LLC include SORRENTO BONE GRAFT SUBSTITUTE.