Medical Device Manufacturer · US , Naperville , IL

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

6 submissions · 4 cleared · Since 1998

Total

Cleared

Denied

Medigroup, Inc. has 4 FDA 510(k) cleared medical devices. Based in Naperville, US.

Historical record: 4 cleared submissions from 1998 to 2012. Primary specialty: Gastroenterology & Urology.

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

Medigroup, Inc. is one of 15071 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

6 devices

1-6 of 6