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.

510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.

FDA 510(k) Regulatory Record - Wandercraft SAS

3 devices

1-3 of 3

Cleared CT Oct 24, 2025

Regulatory Intelligence

Linked clinical trials FDA-regulated device evidence

Regulatory consultant 510(k) submission support ecosystem

Emergo Global Consulting, LLC

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Clinical validation data available

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026

Wandercraft SAS - FDA 510(k) Cleared Devices

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