Sm Eng Co., Ltd.

Sm Eng Co., Ltd. — FDA 510(k) Submissions

Sm Eng Co., Ltd. has submitted 5 FDA 510(k) premarket notifications since 2017, of which 5 received clearance as substantially equivalent to a predicate device.

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