FDA applicant

Wandercraft SAS

Paris, FR4 decisions2022–20261 recall

FDA records 4 decisions for Wandercraft SAS (Paris, FR) from 2022 to 2026: 4 510(k) clearances. All are in product code PHL (Powered Exoskeleton). Its devices cite 6 predicates, 3 of them its own earlier devices. 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Wandercraft SAS’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2022high 1 (2022) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

1in 2025

2022high 1 (2025) · low 0 (2022)2026

Class I Class II/III not classified

FIG. 1 — Wandercraft SAS by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Wandercraft SAS

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?