Medical Device Manufacturer · US , Morrisville , NC

Gentris Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2006

Total

Cleared

Denied

Gentris Corporation has 1 FDA 510(k) cleared medical devices. Based in Morrisville, US.

Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Gentris Corporation Filter by specialty or product code using the sidebar.

Gentris Corporation 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 - Gentris Corporation

1 devices

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