LivaNova USA, Inc.

LivaNova USA, Inc. — FDA 510(k) Submissions

LivaNova USA, Inc. has submitted 3 FDA 510(k) premarket notifications since 2024, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass, Tubing, Pump, Cardiopulmonary Bypass . Use the specialty filter in the sidebar to narrow results.