Ilumark GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Ilumark GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ilumark GmbH has 1 FDA 510(k) cleared medical devices. Based in Muhlheim, DE.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Ilumark GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ilumark GmbH
1 devices