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Bellafill® Dermal FillerP020012

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Bellafill® Dermal Filler is a Hyaluronic acid filler product, registered by Tiger Aesthetics Medical, LLC. Linked registrations: US P020012. First approved in US on 2006-10-27 (P020012). Data as of 2026-10-19.

  • Regulatory classHyaluronic acid filler · class not determined
  • HolderTiger Aesthetics Medical, LLC
  • JurisdictionsUS
  • Updated2026-10-19 · v1

Registration and basics are public; findings and prices need an account

Registration and basics

Bellafill® Dermal Filler

Product
Regulatory class
Not determined (no verified registration linked)Could not verify
Category
Hyaluronic acid filler
US · FDA PMA
P020012
Name on registration
ARTEFILL, BELLAFILL PMMA COLLAGEN PERMANENT DERMAL FILLER
Registrant
Tiger Aesthetics Medical, LLC
First approval
2006-10-27
This certificate issued
2006-10-27
Checked against official page
Not yet checked field by field against the live official page

Public: fields from the registration record.

Label facts by jurisdiction

What each jurisdiction's label says for the same attribute; gaps are marked Not reported, irrelevant ones N/A

No data yet

Registration timeline

  1. US

    P020012 first approved

  2. US

    P020012 · P020012/S046

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜implement the supplier's change to the sterilization method and min…

  3. US

    P020012 · P020012/S047

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Change to implement an alternate shipper (shipping container).

  4. US

    P020012 · P020012/S048

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approval for changes to SDS-PAGE collagen analysis test equipment u…

  5. US

    P020012 · P020012/S049

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜approval for an alternate preservative to be used in the subassembl…

  6. US

    P020012 · P020012/S052

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approval for changes to bulk mixing equipment during subassembly ma…

  7. US

    P020012 · P020012/S051

    Normal 180 Day Track No User Fee｜Labeling Change - Indications/instructions/shelf life/tradename｜Approval to change the device trade name fr…

First approval, this certificate's issue date (updated after renewals or changes), changes and expiry are listed separately; a missing first approval means it was not obtained from an official source. Up to 6 recent changes per registration; click the number for the full record.

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Recent changes

5
  • P020012: Normal 180 Day Track No User Fee｜Labeling Change - Indications/instructions/shel…2026-08-07
  • P020012: 30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approva…2026-05-12
  • P020012: 30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜approva…2025-04-29
  • P020012: 30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approva…2025-01-07
  • P020012: 30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Change …2024-04-26

Sources

1