FDA grants breakthrough device designation for Renovos’ bone graft gel
Renovite BMP-2 is made from a synthetic nanoclay gel, designed to be safer and more effective than current bone graft materials.
UK-based Renovos Biologics has been granted breakthrough device designation from the US Food and Drug Administration (FDA) for Renovite BMP-2 (bone morphogenic protein 2), a synthetic nanoclay bone fusion gel. Renovite BMP-2 is used as an alternative to a bone graft. The gel, which contains a growth factor BMP-2, allows precise bone formation at the specific area. The nanoclay gel ensures safe and targeted bone fusion without BMP-2 leakage, and naturally degrades as new bone forms.
