Biomendex OY

Biomendex OY — FDA 510(k) Submissions

Biomendex OY has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Filler, Bone Void, Calcium Compound . Use the specialty filter in the sidebar to narrow results.