Femasys, Inc.

Femasys, Inc. — FDA 510(k) Submissions

Femasys, Inc. has submitted 9 FDA 510(k) premarket notifications since 2009, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cannula, Manipulator/injector, Uterine, Sampler, Endocervical, Catheter, Assisted Reproduction . Use the specialty filter in the sidebar to narrow results.