ClearanceBrief
Company ยท FR

Wandercraft SAS

FDA 510(k) clearances and medical device recalls filed under this name, 2022 to 2026. Name variants (Inc, Corp, punctuation) are merged.

4510(k) clearances (1 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
PHLPowered Exoskeleton5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 3, 2026K260381Eve
Wandercraft SAS, FR
PHL
Oct 24, 2025K250904Atalante X
Wandercraft SAS, FR
PHL
Dec 13, 2023K232077Atalante X
Wandercraft SAS, FR
PHL
Dec 29, 2022K221859Atalante
Wandercraft SAS, FR
PHL

Latest recalls

DateFirm and productCodeLinked 510(k)
May 8, 2025WANDERCRAFT SAS
Atalante X, Powered Exoskeleton. Atalante X is intended to perform ambulatory functions and mobility exercises, hands-free, in rehabilitation institutions under the supervision of a trained operator.
Open, Classified
PHLK221859
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