Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007410669

FEI Number

3007410669

Entity Name

MAIRE-DIDIER

City/State/Country

Chaumont Haute-Marne, FR

Establishment Address

17 Route De Neuilly, Chaumont Haute-Marne 52000, FR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Maire-Didier (Owner Number: 10037781)

Owner / Operator Contact Address

17 ROUTE DE NEUILLY, CHAUMONT, FR-52 52000, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

OSTEOTOME TEMPLATE extractor IMPACTOR ERGONICS Surgical Instruments

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HWM	Osteotome	General, Plastic Surgery	Class 1	878.4800	2023-02-28
HWN	Instrument, Compression	Orthopedic	Class 1	888.4540	2023-02-28
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2015-01-28
HWT	Template	Orthopedic	Class 1	888.4800	2023-02-28
HXW	Bender	Orthopedic	Class 1	888.4540	2023-02-28
HWB	Extractor	Orthopedic	Class 1	888.4540	2018-06-11
HXX	Screwdriver	Orthopedic	Class 1	888.4540	2023-02-28
HWA	Impactor	Orthopedic	Class 1	888.4540	2023-02-28
DWS	Instruments, Surgical, Cardiovascular	Cardiovascular	Class 1	870.4500	2011-08-15
JAC	System, X-Ray, Film Marking, Radiographic	Radiology	Class 1	892.1640	2024-01-04
HXB	Probe	Orthopedic	Class 1	888.4540	2023-02-28

Official Correspondent

Servan Ouin

US Agent Details

Michael Crawford Business: MED ALLIANCE Email: info@medallianceinternational.com Phone: (630) 4437070

Related Public Records

Same Entity

Maire-Didier

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011	Depuy Orthopaedics, Inc.	1	Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

Similar Registrations

Registration Number	Establishment Name	Location
3007507973	ADLER INSTRUMENT COMPANY	Brooksville, FL, US
8010379	DEPUY INTL., LTD.	LEEDS, GB
9616671	DEPUY (IRELAND)	CO. CORK Munster, IE
3002862271	Wenzler Medizintechnik GmbH	Frittlingen Baden-Wurttemberg, DE
1926681	JEDMED Instrument Company	Saint Louis, MO, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007410669. Last updated year: 2026. Please use registration number 3007410669 when referencing this establishment in official correspondence.