Medical Device Manufacturer · US , San Diego , CA

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

2 submissions · 2 cleared · Since 2009

Total

Cleared

Denied

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

Historical record: 2 cleared submissions from 2009 to 2014. Primary specialty: General & Plastic Surgery.

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

Synthasome, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Synthasome, Inc. — FDA 510(k) Products and Clearance History

2 devices

1-2 of 2