Auxogyn, Inc.

Auxogyn, Inc. — FDA 510(k) Submissions

Auxogyn, Inc. has submitted 4 FDA 510(k) premarket notifications since 2011, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Embryo Image Assessment System, Assisted Reproduction, Labware, Assisted Reproduction . Use the specialty filter in the sidebar to narrow results.