Bredent GmbH & Co. KG is one of 467 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Bredent GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: visio.lign color, visio.lign shield, BioHPP - breCAM.BioHPP, BREDENT NOVO.LIGN A/ BREDENT NOVO.LIGN P
3
Total
3
Cleared
0
Denied
Bredent GmbH & Co. KG has 3 FDA 510(k) cleared medical devices. Based in Tuttlingen, Baden Wurttemberg, DE.
Latest FDA clearance: Dec 2024. Active since 2010. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bredent GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bredent GmbH & Co. KG
3 devices