Kbl GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Kbl GmbH - FDA 510(k) Cleared Devices
Recent clearances: KBL 7000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL 8000 alpha hybridSun
1
Total
1
Cleared
0
Denied
Kbl GmbH has 1 FDA 510(k) cleared medical devices. Based in Dernbach, DE.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kbl GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kbl GmbH
1 devices