Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003192334

FEI Number

3003192334

Entity Name

SUTUREX & RENODEX S.A.

City/State/Country

CARSAC AILLAC Dordogne, FR

Establishment Address

ZAE du Perigord Noir, 4, rue Jacques Chemel, CARSAC AILLAC Dordogne 24200, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SUTUREX & RENODEX (Owner Number: 9074199)

Owner / Operator Contact Address

ZAE du Perigord Noir, 4, rue Jacques Chemel, CARSAC AILLAC, FR-24 24200, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SUTUREX & RENODEX S.A.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GAB	Needle, Suturing, Disposable	General, Plastic Surgery	Class 1	878.4800	2005-06-15

Official Correspondent

Oriane MOREAU

US Agent Details

Kamaal Anas Business: Aesculap, Inc. Email: kamaal.anas@bbraunusa.com Phone: (610) 9849071

Related Public Records

Same Entity

SUTUREX & RENODEX

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 3003192334. Last updated year: 2026. Please use registration number 3003192334 when referencing this establishment in official correspondence.