MEDICATECHNOLOGIE

FDA Device Registration & Listing · CHARTRES-DE-BRETAGNE Ille-et-Vilaine, FR · Registration 3010389204

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
3010389204
FEI Number
3010389204
Entity Name
MEDICATECHNOLOGIE
City/State/Country
CHARTRES-DE-BRETAGNE Ille-et-Vilaine, FR
Establishment Address
28, rue du village de la metairie, CHARTRES-DE-BRETAGNE Ille-et-Vilaine 35131, FR
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
MEDICATECHNOLOGIE (Owner Number: 10043789)
Owner / Operator Contact Address
28, RUE DU VILLAGE DE LA METAIRIE, CHARTRES-DE-BRETAGNE, FR-35 35131, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Airlock Centrolock Novastep

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2020-01-07
JDR Staple, Fixation, Bone Orthopedic Class 2 888.3030 2017-12-29
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2017-12-29
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2019-03-06
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment General, Plastic Surgery Class 1 878.4820 2017-12-29

Official Correspondent

No official correspondent registered.

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

MEDICATECHNOLOGIE
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K042598 Zimmer, Inc. PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES 2004-10-29
K190842 Jiangsu Trauhui Medical Instrument Co., Ltd. Comus Locking Plate systems 2020-02-03
K130510 Arthrex, Inc. ARTHREX COMPRESSION PLATES 2013-09-25
K202803 Newclip Technics Activmotion S DTO 2021-12-16
K153770 In2bones Sas OS2(R)-VP Varisation Staple 2016-03-21

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0034-2022 Flower Orthopedics Corporation 2
Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
Z-0008-2023 Synthes (USA) Products LLC 2
Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001
Z-0013-05 Biomet, Inc. 2
Lactosorb pin, 2.0 x 20 mm, sterile; ref. 948205.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010389204. Last updated year: 2026. Please use registration number 3010389204 when referencing this establishment in official correspondence.
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