Medentis Medical GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Medentis Medical GmbH - FDA 510(k) Cleared Devices
Recent clearances: ICX-Implant System
1
Total
1
Cleared
0
Denied
Medentis Medical GmbH has 1 FDA 510(k) cleared medical devices. Based in Bad Neuenahr-Ahrweiler, DE.
Latest FDA clearance: Sep 2024. Active since 2024. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Medentis Medical GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by PaxMed International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Medentis Medical GmbH
1 devices