Medical Device Manufacturer · US , Minneapolis , MN

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

3 submissions · 2 cleared · Since 2013

Total

Cleared

Denied

Iogyn, Inc. has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: Obstetrics & Gynecology.

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

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

3 devices

1-3 of 3