WANDERCRAFT SAS
WANDERCRAFT SAS appears in FDA public data with 1 recall, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1739-2025, Class II) was initiated on April 3, 2025. Its most recent 510(k) clearance was granted on October 24, 2025.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1739-2025 | Class II | Atalante X, Powered Exoskeleton. Atalante X is intended to perform ambulatory functions and mobili | April 3, 2025 |