ALLPACK GROUP AG

FDA Device Registration & Listing · Reinach Basel-Landschaft, CH · Registration 3010164402

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
3010164402
FEI Number
3007517952
Entity Name
ALLPACK GROUP AG
City/State/Country
Reinach Basel-Landschaft, CH
Establishment Address
Kaegenstrasse 17, Reinach Basel-Landschaft 4153, CH
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Allpack Group AG (Owner Number: 10039512)
Owner / Operator Contact Address
Pfeffingerstrasse 45, Reinach, CH-BL 4153, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number

All Registered Proprietary Names

Belotero Balance®

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 2012-01-18

Official Correspondent

Michael Paulisch

US Agent Details

Ellen Iwudibia Business: Biologics Consulting Email: eiwudibia@biologicsconsulting.com Phone: (703) 7395695

Related Public Records

Same Entity

Allpack Group AG
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004362706 ALLPACK GROUP AG Reinach Basel-Landschaft, CH

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010164402. Last updated year: 2026. Please use registration number 3010164402 when referencing this establishment in official correspondence.
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