Aurolab

Aurolab — FDA 510(k) Submissions

Aurolab has submitted 4 FDA 510(k) premarket notifications since 2003, of which 4 received clearance as substantially equivalent to a predicate device.

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