Bego Implant Systems GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Bego Implant Systems GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: BEGO SEMADOS Tr 58350, BEGO Semados® RS/RSX Implant System
3
Total
3
Cleared
0
Denied
Bego Implant Systems GmbH & Co. KG has 3 FDA 510(k) cleared medical devices. Based in Bremen, DE.
Last cleared in 2021. Active since 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bego Implant Systems GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bego Implant Systems GmbH & Co. KG
3 devices