Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003677417

FEI Number

3003677417

Entity Name

ACTEON MANUFACTURING

City/State/Country

Merignac Gironde, FR

Establishment Address

Zone Industrielle Du Phare, 17 Av Gustave Eiffel, Merignac Gironde 33700, FR

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

ACTEON MANUFACTURING (Owner Number: 9069839)

Owner / Operator Contact Address

Zone Industrielle Du Phare, 17 Av Gustave Eiffel, MERIGNAC, FR-33 33700, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K050180

PMA Number

N/A

All Registered Proprietary Names

EXPASYL EXACT EXPASYL

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MVL	Cord, Retraction	Unknown	Class U	N/A	2007-10-11

Official Correspondent

Genenieve Devilledon

US Agent Details

Noelle Zuccarello Business: Acteon, Inc Email: noelle.zuccarello@acteongroup.com Phone: (800) 2896367

Related Public Records

Same Entity

ACTEON MANUFACTURING

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 3003677417. Last updated year: 2026. Please use registration number 3003677417 when referencing this establishment in official correspondence.