Blue Sky Bio

Blue Sky Bio — FDA 510(k) Submissions

Blue Sky Bio has submitted 5 FDA 510(k) premarket notifications since 2000, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Endosseous, Root-form, Bone Grafting Material, Synthetic, Powder, Porcelain, Bracket, Plastic, Orthodontic . Use the specialty filter in the sidebar to narrow results.