Medical Device Manufacturer · US , Fountain Valley , CA

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

5 submissions · 5 cleared · Since 2000

Total

Cleared

Denied

Sutura, Inc. has 5 FDA 510(k) cleared medical devices. Based in Fountain Valley, US.

Historical record: 5 cleared submissions from 2000 to 2006. Primary specialty: General & Plastic Surgery.

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

Sutura, Inc. is one of 15074 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5