Medical Device Manufacturer · MX , Mexico City

Clemde SA DE CV

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

Clemde SA DE CV — FDA 510(k) Submissions

Clemde SA DE CV 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 Resin, Denture, Relining, Repairing, Rebasing . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Dental 2