Medical Device Manufacturer · US , Hopkonton , MA

Suturtek Incorporated - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2003

Total

Cleared

Denied

Suturtek Incorporated has 4 FDA 510(k) cleared medical devices. Based in Hopkonton, US.

Historical record: 4 cleared submissions from 2003 to 2008. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Suturtek Incorporated Filter by specialty or product code using the sidebar.

Suturtek Incorporated is one of 21783 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Suturtek Incorporated

4 devices

1-4 of 4