Medical Device Manufacturer · US , Mchenry , IL

Gentex Corporation - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1977

Total

Cleared

Denied

Gentex Corporation has 3 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 3 cleared submissions from 1977 to 2009. Primary specialty: Ophthalmic.

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

Gentex 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 - Gentex Corporation

3 devices

1-3 of 3