Medical Device Manufacturer · US , Menlo Park , CA

Auxogyn, Inc. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 2011

Total

Cleared

Denied

Auxogyn, Inc. has 3 FDA 510(k) cleared medical devices. Based in Menlo Park, US.

Historical record: 3 cleared submissions from 2011 to 2014. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Auxogyn, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Auxogyn, Inc.

4 devices

1-4 of 4