Demetech Corp.

Demetech Corp. — FDA 510(k) Submissions

Demetech Corp. has submitted 10 FDA 510(k) premarket notifications since 2002, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Absorbable, Synthetic, Polyglycolic Acid, Suture, Absorbable, Natural, Suture, Surgical, Absorbable, Polydioxanone, Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile, Suture, Nonabsorbable, Synthetic, Polyamide . Use the specialty filter in the sidebar to narrow results.