ALLERGAN

FDA Device Registration & Listing · Annecy Haute-Savoie, FR · Registration 3005113652

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005113652
FEI Number
3005113652
Entity Name
ALLERGAN
City/State/Country
Annecy Haute-Savoie, FR
Establishment Address
Rte De Promery - ZA de Pre Mairy, Pringy, Annecy Haute-Savoie 74370, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AbbVie, Inc. (Owner Number: 2011068)
Owner / Operator Contact Address
2525 DUPONT DRIVE, --, Irvine, CA 92612, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number

All Registered Proprietary Names

Juvederm Ultra Juvederm Ultra XC Juvederm Ultra Plus Juvederm 30 Juvederm Ultra Plus XC Juvederm Voluma XC Juvederm Volbella XC Juvederm Volux XC Juvederm Vollure XC Skinvive by Juvederm

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2015-01-23
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2015-01-23

Official Correspondent

James Wabby

US Agent Details

James Wabby Business: ABBVIE, INC. Email: james.wabby@abbvie.com Phone: (714) 2462259

Related Public Records

Same Entity

AbbVie, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
1643525 ALLERGAN SALES, LLC WACO, TX, US
3013307971 ABBVIE Logistics BV, Inc Zwolle Overijssel, NL
8020862 ALLERGAN PHARMACEUTICALS IRELAND WESTPORT Mayo, IE
1647098 LIFECELL CORP. BRANCHBURG, NJ, US
9617229 ALLERGAN LA AURORA DE HEREDIA, CR

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005113652. Last updated year: 2026. Please use registration number 3005113652 when referencing this establishment in official correspondence.
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