Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3033557295

FEI Number

3033557295

Entity Name

HOPPER

City/State/Country

Albi Tarn, FR

Establishment Address

8 Avenue Pierre Gilles de Gennes, Albi Tarn 81000, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Hopper (Owner Number: 10091506)

Owner / Operator Contact Address

8 Avenue Pierre Gilles de Gennes, Albi, FR-81 81000, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Audacieuse by Hopper Foot, Intrepide by Hopper Foot

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISH	Component, External, Limb, Ankle/Foot	Physical Medicine	Class 1	890.3420	2024-10-10

Official Correspondent

Victor Premaud

US Agent Details

Michael Dennison Business: Proteor USA Email: michael.dennison@proteor.com Phone: (602) 6419402

Related Public Records

Same Entity

Hopper

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033557295. Last updated year: 2026. Please use registration number 3033557295 when referencing this establishment in official correspondence.