Auxogyn, Inc. is one of 13055 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Auxogyn, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EEVA SYSTEM, EEVA DISH (WITH 12 MICROWELLS)
4
Total
3
Cleared
1
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.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Auxogyn, Inc.
4 devices