Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007744205

FEI Number

3007744205

Entity Name

ANTEIS SA

City/State/Country

Plan les ouates Geneve, CH

Establishment Address

Chemin des aulx 12, Plan les ouates Geneve 1228, CH

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Anteis SA (Owner Number: 10029433)

Owner / Operator Contact Address

Chemin d'Etraz 2, 1027 Lonay, Lonay, CH-VD 1027, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P250020

All Registered Proprietary Names

Belotero Balance Belotero Balance (+) Lidocaine Belotero Volume (+) Lidocaine

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	2012-01-13
LMH	Implant, Dermal, For Aesthetic Use	Unknown	Class 3	N/A	2026-05-27

Official Correspondent

Esteban Uriarte

US Agent Details

Micki Lew Business: Merz North America, Inc Email: micki.lew@merz.com Phone: (919) 6915943

Related Public Records

Same Entity

Anteis SA

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 3007744205. Last updated year: 2026. Please use registration number 3007744205 when referencing this establishment in official correspondence.