Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3001169357

FEI Number

3001169357

Entity Name

MEDI-LINE S.A.

City/State/Country

Angleur Liege, BE

Establishment Address

rue des Gardes-frontieres, 5, Angleur Liege 4031, BE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

MEDI-LINE S.A. (Owner Number: 10085554)

Owner / Operator Contact Address

rue des Gardes-frontieres, 5, Angleur, BE-WLG 4031, BE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Endomina system

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OCW	Endoscopic Tissue Approximation Device	Gastroenterology, Urology	Class 2	876.1500	2022-07-01

Official Correspondent

Christophe ANISET

US Agent Details

Mindy McCann Business: Qserve Group US, Inc. Email: USagent@qservegroup.com Phone: (424) 2718169

Related Public Records

Same Entity

MEDI-LINE S.A.

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
K082659	Covidien Lp, Formerly Registered AS United States	MODIFIED ENDO STICH	2008-09-19

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001169357. Last updated year: 2026. Please use registration number 3001169357 when referencing this establishment in official correspondence.