Kbl AG is one of 199 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Kbl AG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kbl AG has 1 FDA 510(k) cleared medical devices. Based in Dernbach, DE.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kbl AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kbl AG
1 devices