EvoEndo, Inc.

EvoEndo, Inc. — FDA 510(k) Submissions

EvoEndo, Inc. has submitted 3 FDA 510(k) premarket notifications since 2022, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Gastroscope And Accessories, Flexible/rigid . Use the specialty filter in the sidebar to narrow results.