Demetech Corporation

Demetech Corporation — FDA 510(k) Submissions

Demetech Corporation has submitted 5 FDA 510(k) premarket notifications since 2018, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Surgical, Absorbable, Polydioxanone, Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene, Suture, Nonabsorbable, Synthetic, Polyethylene, Mask, Surgical . Use the specialty filter in the sidebar to narrow results.