Brivant Limited is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Brivant Limited - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Brivant Limited has 2 FDA 510(k) cleared medical devices. Based in Oranmore, Galway, IE.
Historical record: 2 cleared submissions from 2006 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Brivant Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Brivant Limited
2 devices