Medical Device Manufacturer · US , Avondale , AZ

Suretex, Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1991

Total

Cleared

Denied

Suretex, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Avondale, US.

Historical record: 5 cleared submissions from 1991 to 2003. Primary specialty: Obstetrics & Gynecology.

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

Suretex, Ltd. 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 - Suretex, Ltd.

5 devices

1-5 of 5