Medical Device Manufacturer · FR , Paris

Wandercraft SAS - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2022

Total

Cleared

Denied

Wandercraft SAS has 3 FDA 510(k) cleared medical devices. Based in Paris, FR.

Latest FDA clearance: Oct 2025. Active since 2022. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Wandercraft SAS

3 devices

1-3 of 3