Incereb, Ltd. is one of 45 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Incereb, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Incereb, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Dublin, IE.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Incereb, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Incereb, Ltd.
1 devices