Medical Device Manufacturer · DE , Bonn

Ceramoptec GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ceramoptec GmbH General & Plastic Surgery ✕
2 devices
1-2 of 2
Cleared Jul 14, 2025
Leonardo Duster
K250504 · GEX
General & Plastic Surgery · 144d
Cleared Sep 01, 2021
Leonardo Mini Blue
K210951 · GEX
General & Plastic Surgery · 155d
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All2 General & Plastic Surgery 2