Medical Device Manufacturer · FR , Paris

Milvue - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2024
2
Total
2
Cleared
0
Denied

Milvue has 2 FDA 510(k) cleared medical devices. Based in Paris, FR.

Latest FDA clearance: Jan 2025. Active since 2024. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Milvue Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Cosm and Hogan Lovells US LLP.

FDA 510(k) Regulatory Record - Milvue
2 devices
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