Medical Device Manufacturer · US , Menlo Park , CA

Auxogyn, Inc.

4 submissions · 3 cleared · Since 2011
4
Total
3
Cleared
1
Denied

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.

4 devices
1–4 of 4
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