Medart A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Medart A/S - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Medart A/S has 3 FDA 510(k) cleared medical devices. Based in Hvidovre, DK.
Historical record: 3 cleared submissions from 2009 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medart A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medart A/S
3 devices