Medical Device Manufacturer · US , Deerfield , IL

Omnis Surgical, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1985

Total

Cleared

Denied

Omnis Surgical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Deerfield, US.

Historical record: 4 cleared submissions from 1985 to 1985. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Omnis Surgical, Inc.

4 devices

1-4 of 4