Serral, S.A. DE C.V.

Serral, S.A. DE C.V. — FDA 510(k) Submissions

Serral, S.A. DE C.V. has submitted 6 FDA 510(k) premarket notifications since 2002, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Nonabsorbable, Synthetic, Polyamide, Suture, Nonabsorbable, Synthetic, Polypropylene, Suture, Absorbable, Natural, Suture, Nonabsorbable, Silk, Suture, Nonabsorbable, Synthetic, Polyethylene . Use the specialty filter in the sidebar to narrow results.