Orgentec Diagnostika GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orgentec Diagnostika GmbH - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Orgentec Diagnostika GmbH has 3 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 3 cleared submissions from 2003 to 2010. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Orgentec Diagnostika GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Orgentec Diagnostika GmbH
3 devices