Xenocor, Inc.

Xenocor, Inc. — FDA 510(k) Submissions

Xenocor, Inc. has submitted 5 FDA 510(k) premarket notifications since 2016, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery . Use the specialty filter in the sidebar to narrow results.