Ontex Sante France SAS

FDA Device Registration & Listing · Dourges Hauts-de-France, FR · Registration 3013684440

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
3013684440
FEI Number
3013684440
Entity Name
Ontex Sante France SAS
City/State/Country
Dourges Hauts-de-France, FR
Establishment Address
Quai du Rivage, Dourges Hauts-de-France 62119, FR
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Ontex Mexico Operations S.A de C.V (Owner Number: 9036701)
Owner / Operator Contact Address
Calle Doce Norte 105, Ciudad Industrial, Tijuana, MX-BCN 22444, MX
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2003-02-27

Official Correspondent

Cecilia Guadalupe Jimenez Rodriguez

US Agent Details

Kyna Smith Business: Valor Brands LLC Email: kyna.smith@ontexglobal.com Phone: (770) 3469250

Related Public Records

Same Entity

Ontex Mexico Operations S.A de C.V
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3010220314 ONTEX MEXICO OPERATIONS SA DE CV Tijuana Baja California, MX
3003500682 ONTEX CZ S.R.O. TURNOV Liberec, CZ
9617256 ONTEX PENINSULAR SAU SEGOVIA, ES
3003449471 Ontex Eeklo Eeklo Oost-Vlaanderen, BE
3012409274 Ontex Manufacturing Italy SRL Ortona Chieti, IT

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013684440. Last updated year: 2026. Please use registration number 3013684440 when referencing this establishment in official correspondence.
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