Vipamat Sarl is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Vipamat Sarl - FDA 510(k) Cleared Devices
Recent clearances: Hippocampe Marathon and Trail
1
Total
1
Cleared
0
Denied
Vipamat Sarl has 1 FDA 510(k) cleared medical devices. Based in Ploemeur, FR.
Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Vipamat Sarl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Rook Quality Systems, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Vipamat Sarl
1 devices