Medical Device Manufacturer · DE , Brehna

mibeTec GmbH

2 submissions · 2 cleared · Since 2022
2
Total
2
Cleared
0
Denied

mibeTec GmbH — FDA 510(k) Submissions

mibeTec GmbH has submitted 2 FDA 510(k) premarket notifications since 2022, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pad, Heating, Powered . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Physical Medicine 2