Wandercraft Incorporated

FDA Device Registration & Listing · New York, NY, US · Registration 3034724466

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3034724466
FEI Number
3034724466
Entity Name
Wandercraft Incorporated
City/State/Country
New York, NY, US
Establishment Address
345 Park Ave S, New York, NY 10010, US
Establishment Type(s)
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
N
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

No US Agent registered (Local establishment).

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
3015000676 WANDERCRAFT Paris Ile-de-France, FR

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3034724466. Last updated year: 2026. Please use registration number 3034724466 when referencing this establishment in official correspondence.
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