Medical Device Manufacturer · US , Austin , TX

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

5 submissions · 5 cleared · Since 1994

Total

Cleared

Denied

Surgiquip, Inc. has 5 FDA 510(k) cleared medical devices. Based in Austin, US.

Historical record: 5 cleared submissions from 1994 to 1994. Primary specialty: General & Plastic Surgery.

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

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

5 devices

1-5 of 5