Gentian AS is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gentian AS - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Gentian AS has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 2 cleared submissions from 2007 to 2008. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Gentian AS Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gentian AS
2 devices