Medical Device Manufacturer · CH , Renens

Lumendo AG

2 submissions · 2 cleared · Since 2023
2
Total
2
Cleared
0
Denied

Lumendo AG — FDA 510(k) Submissions

Lumendo AG has submitted 2 FDA 510(k) premarket notifications since 2023, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laser Activator For Polymerization, Resin, Root Canal Filling . Use the specialty filter in the sidebar to narrow results.

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