Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022505496

FEI Number

3022505496

Entity Name

TRANSLUMINAL

City/State/Country

pompey Meurthe-et-Moselle, FR

Establishment Address

80 boulevard de la moselle, pompey Meurthe-et-Moselle 54340, FR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

transluminal (Owner Number: 10085068)

Owner / Operator Contact Address

80 boulevard de la moselle, pompey, FR-54 54340, FR

Initial Importer Flag

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
OCW	Endoscopic Tissue Approximation Device	Gastroenterology, Urology	Class 2	876.1500	2022-05-02

Official Correspondent

jean-baptiste pourchet

US Agent Details

Nathan Remsberg Email: nathan.remsberg@saint-gobain.com Phone: (734) 8347935

Related Public Records

Same Entity

transluminal

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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3021632375	IVUS ILAC SANAYI VE TICARET AS	Istanbul, TR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022505496. Last updated year: 2026. Please use registration number 3022505496 when referencing this establishment in official correspondence.