Data / Medical devices / Switzerland / Allpack Group AG
Allpack Group AG: FDA-registered device maker in Reinach Basel-Landschaft, Switzerland, 1 PMA approval
Allpack Group AG is registered with the FDA (registration 3010164402) in Reinach Basel-Landschaft, Switzerland. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated November 14, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010164402
- FEI number
- 3007517952
- Address
- Kaegenstrasse 17, Reinach Basel-Landschaft, Switzerland, 4153
- Owner or operator
- Allpack Group AG (10039512)
- Roles
- Repackager or relabeler
- First device listed
- January 18, 2012
- Registered through
- 2026
- Brand names listed
- Belotero Balance®
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Implant, Dermal, For Aesthetic Use | LMH | 3 | Repackager or relabeler | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| November 14, 2011 | P090016 | BELOTERO BALANCE | LMH | 60 | May 3, 2026 | accessdata.fda.gov |
Compare with other makers
Updated May 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.