Medical Device Manufacturer · US , Roswell , GA

Genexel-Sein, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2007

Total

Cleared

Denied

Genexel-Sein, Inc. has 2 FDA 510(k) cleared medical devices. Based in Roswell, US.

Historical record: 2 cleared submissions from 2007 to 2009. Primary specialty: Cardiovascular.

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

Genexel-Sein, 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 - Genexel-Sein, Inc.

2 devices

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