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510k Database
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CH
Modela AG
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Medical Device Manufacturer
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CH , Baar
Modela AG - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2017
Recent clearances:
Basic, Dominant Flex
View 1 510(k) Devices ↓
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Modela AG
General & Plastic Surgery
✕
1
devices
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Cleared
Mar 24, 2017
Basic, Dominant Flex
K170329
·
QPB
General & Plastic Surgery
·
50d
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General & Plastic Surgery
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