mibeTec GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
mibeTec GmbH - FDA 510(k) Cleared Devices
Recent clearances: bite away two, bite away neo
2
Total
2
Cleared
0
Denied
mibeTec GmbH has 2 FDA 510(k) cleared medical devices. Based in Brehna, DE.
Latest FDA clearance: Sep 2025. Active since 2022. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by mibeTec GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by QSR Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - mibeTec GmbH
2 devices