Cypris Medical

Cypris Medical — FDA 510(k) Submissions

Cypris Medical has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

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