Medical Device Manufacturer · US , Westlake , OH

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

6 submissions · 6 cleared · Since 2016

Total

Cleared

Denied

Surgtech, Inc. has 6 FDA 510(k) cleared medical devices. Based in Westlake, US.

Historical record: 6 cleared submissions from 2016 to 2019. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by Orchid Design as regulatory consultant.

Surgtech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

6 devices

1-6 of 6