Kline Europe GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kline Europe GmbH has 1 FDA 510(k) cleared medical devices. Based in Dusseldorf, DE.
Last cleared in 2022. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Kline Europe GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Kline Europe GmbH
1 devices