Medical Device Manufacturer · US , Garden Grove , CA

Quality Synthetics Intl, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1988

Total

Cleared

Denied

Quality Synthetics Intl, Inc. has 4 FDA 510(k) cleared medical devices. Based in Garden Grove, US.

Historical record: 4 cleared submissions from 1988 to 1990. Primary specialty: Obstetrics & Gynecology.

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

Quality Synthetics Intl, 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 - Quality Synthetics Intl, Inc.

4 devices

1-4 of 4