Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015000676

FEI Number

3015000676

Entity Name

WANDERCRAFT

City/State/Country

Paris Ile-de-France, FR

Establishment Address

88 rue de Rivoli, Paris Ile-de-France 75004, FR

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Wandercraft (Owner Number: 10087464)

Owner / Operator Contact Address

88 rue de Rivoli, Paris, FR-IDF 75004, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K221859

PMA Number

N/A

All Registered Proprietary Names

Atalante X Atalante X Atalante X Atalante

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PHL	Powered Exoskeleton	Physical Medicine	Class 2	890.3480	2025-12-25
PHL	Powered Exoskeleton	Physical Medicine	Class 2	890.3480	2023-12-21
PHL	Powered Exoskeleton	Physical Medicine	Class 2	890.3480	2023-03-02

Official Correspondent

Maria Ida Iacono

US Agent Details

Matthieu Masselin Email: matthieu@wandercraft.health Phone: (929) 5982020

Related Public Records

Same Entity

Wandercraft

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3034724466	Wandercraft Incorporated	New York, NY, US

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3034724466	Wandercraft Incorporated	New York, NY, US
3007615665	Lifeward LTD.	Upper Yokneam Northern, IL

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015000676. Last updated year: 2026. Please use registration number 3015000676 when referencing this establishment in official correspondence.