Medical Device Manufacturer · FR , Ploemeur

Vipamat Sarl - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
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
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All1 Physical Medicine 1