Wandercraft SAS is one of 271 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Wandercraft SAS - FDA 510(k) Cleared Devices
Recent clearances: Eve, Atalante X, Atalante X
4
Total
4
Cleared
0
Denied
Wandercraft SAS has 4 FDA 510(k) cleared medical devices. Based in Paris, FR.
Latest FDA clearance: Aug 2026. 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.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant. 2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Wandercraft SAS
4 devices