Opsens, Inc.

Opsens, Inc. — FDA 510(k) Submissions

Opsens, Inc. has submitted 10 FDA 510(k) premarket notifications since 2015, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Transducer, Pressure, Catheter Tip, Wire, Guide, Catheter . Use the specialty filter in the sidebar to narrow results.