mibeTec GmbH - FDA 510(k) Cleared Devices
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.
2 devices