Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000422168

FEI Number

1000422168

Entity Name

Movmedix S.A.S

City/State/Country

ARC SUR TILLE Bourgogne-Franche-Comte, FR

Establishment Address

5 rue de la Fontaine, ARC SUR TILLE Bourgogne-Franche-Comte 21560, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Movmedix S.A.S (Owner Number: 10062026)

Owner / Operator Contact Address

5 rue de la Fontaine, ARC SUR TILLE, FR-NOTA 21560, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

K-wire Diam. 2 x 150 mm, 2 blunt ends - U01017 Wire Loop 0.5x400 - U014011 Acromio-clavicular guide - B24000 Hexagonal screwdriver 3.5mm - ATVS35 Drilling guide - D03003 Drill bit Diam. 3.5 x 150 mm - U01110 Drill bit Diam. 4.5 x 150 mm - U01101

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2025-09-26
HXI	Passer, Wire, Orthopedic	Orthopedic	Class 1	888.4540	2025-09-26
HXX	Screwdriver	Orthopedic	Class 1	888.4540	2025-09-26
FZX	Guide, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2025-09-26
HTW	Bit, Drill	Orthopedic	Class 1	888.4540	2025-09-26

Official Correspondent

No official correspondent registered.

US Agent Details

Marilyne Joly Business: LOK USA, Inc. Email: regulatory@lok-northamerica.com Phone: (412) 2851076

Related Public Records

Same Entity

Movmedix S.A.S

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

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3038207124	NATIVE ORTHOPAEDICS	Providence, RI, US
3027516563	STAR SPORTS MEDICINE CO., LTD.	Beijing, CN
3021574846	3D LOGICS LLC	Hillsboro, OR, US
3030089866	ORTOLOG MEDIKAL SANAYI VE TICARET A.S.	Yenimahalle Ankara, TR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000422168. Last updated year: 2026. Please use registration number 1000422168 when referencing this establishment in official correspondence.