Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3000254998

FEI Number

3000254998

Entity Name

VEDA LAB

City/State/Country

ALENCON, CEDEX Orne, FR

Establishment Address

RUE DEL EXPANSION,, ZAT DU LONDEAU CERISE, ALENCON, CEDEX Orne 61006, FR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

VEDA LAB (Owner Number: 9025559)

Owner / Operator Contact Address

RUE DEL'EXPANSION,, ZAT DU LONDEAU CERISE, ALENCON, CEDEX, FR-NOTA 61006, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Syphilis Health Check

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LIP	Enzyme Linked Immunoabsorption Assay, Treponema Pallidum	Microbiology	Class 2	866.3830	2013-01-10

Official Correspondent

Raphael Donati

US Agent Details

Norman Proulx Business: Diagnostics Direct, LLC Email: NProulx@diagnosticsdirect2u.com Phone: (609) 3686912

Related Public Records

Same Entity

VEDA LAB

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 3000254998. Last updated year: 2026. Please use registration number 3000254998 when referencing this establishment in official correspondence.