Medical Device Manufacturer · US , San Diego , CA

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

2 submissions · 2 cleared · Since 1990

Total

Cleared

Denied

Syngene, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 2 cleared submissions from 1990 to 1990. Primary specialty: Microbiology.

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

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

2 devices

1-2 of 2