Durastat, LLC

Durastat, LLC — FDA 510(k) Submissions

Durastat, LLC has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.

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