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JuvédermJuvederm

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Juvéderm is a Hyaluronic acid filler product, registered by Allergan. Linked registrations: US P110033, US P050047. First approved in US on 2013-10-22 (P110033). Data as of 2026-11-09.

  • Regulatory classHyaluronic acid filler · class not determined
  • HolderAllergan
  • JurisdictionsUS
  • Updated2026-11-09 · v1

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

Registration and basics

Juvéderm

Product
Regulatory class
Not determined (no verified registration linked)Could not verify
Category
Hyaluronic acid filler
US · FDA PMA
P110033 (link pending review)
US · FDA PMA
P050047 (link pending review)
Name on registration
JUVEDERM VOLUMA XC
Registrant
Allergan
First approval
2013-10-22
Checked against official page
Not yet checked field by field against the live official page

Public: fields from the registration record.Registrant and dates are from P110033; 2 registrations linked.This product record is still pending review.

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

    P050047 first approved

  2. US

    P110033 first approved

  3. US

    P050047 · P050047/S102

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜approval for an additional quality control step during the manufact…

  4. US

    P050047 · P050047/S103

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜undefined

  5. US

    P110033 · P110033/S085

    Normal 180 Day Track｜Change Design/Components/Specifications/Material｜for changes to optimize the Juvederm manufacturing processes.

  6. US

    P110033 · P110033/S100

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜a change in location for manufacturing the tip cap component

  7. US

    P050047 · P050047/S104

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜a change in location for manufacturing the tip cap component

  8. US

    P110033 · P110033/S101

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜to update the varnish used in the manufacture of Juvederm carton bo…

  9. US

    P050047 · P050047/S105

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜to update the varnish used in the manufacture of Juvederm carton bo…

  10. US

    P110033 · P110033/S099

    Panel Track｜Labeling Change - Indications/instructions/shelf life/tradename｜SKINVIVE by JUVÉDERM® is indicated for intradermal injection to …

  11. US

    P110033 · P110033/S091

    Normal 180 Day Track｜Change Design/Components/Specifications/Material｜Approval for using the sodium hyaluronate manufactured from HTL’s addi…

  12. US

    P050047 · P050047/S098

    Normal 180 Day Track｜Change Design/Components/Specifications/Material｜Approval for using the sodium hyaluronate manufactured from HTL’s addi…

  13. US

    P110033 · P110033/S102

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approval for an automated Manufacturing Execution System used for t…

  14. US

    P050047 · P050047/S107

    30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approval for an automated Manufacturing Execution System used for t…

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. Dates on non-Chinese registrations keep the source's wording: UK devices show the registration date (MHRA does not approve them), Australia the ARTG start date, FDA devices the decision date.

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Recent changes

5
  • P110033: 30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approva…2026-08-28
  • P050047: 30-Day Notice｜Process Change - Manufacturer/Sterilizer/Packager/Supplier｜Approva…2026-08-28
  • P110033: Normal 180 Day Track｜Change Design/Components/Specifications/Material｜Approval f…2026-08-11
  • P050047: Normal 180 Day Track｜Change Design/Components/Specifications/Material｜Approval f…2026-08-11
  • P110033: Panel Track｜Labeling Change - Indications/instructions/shelf life/tradename｜SKIN…2026-06-11

Sources

2