Milvue is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Milvue - FDA 510(k) Cleared Devices
Recent clearances: TechCare Trauma, SmartChest
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