Family profileClinically reviewed · indexable

Juvéderm

AbbVie (Allergan Aesthetics)

A family-level profile linking named Juvéderm variants in the operational catalogue to an official manufacturer overview.

Evidence status: Evidence dossier · named clinical review approved

Identity record

What is recorded

v2026.08.15.1
Record type
Source-linked family profile
Recorded maker
AbbVie (Allergan Aesthetics)
Classification
Dermal filler
Material identity
hyaluronic acid
Snapshot date
14 August 2026

Manufacturer and category are catalogue fields. They are not, by themselves, a regulatory classification or verification of the exact marketed presentation.

Names and markets

Aliases in this profile

  • Juvederm

    Unaccented catalogue spelling

Alias grouping supports discovery. It does not claim that regional products, labels, units, formulations, or authorised uses are interchangeable.

Jurisdiction map

What each market source establishes

Ready for clinical review

Product names and regulatory context do not travel automatically between countries. Each row below is limited to its named source market.

US

United States

Regulator record

Named record

JUVEDERM gel implants · JUVÉDERM collection

The FDA PMA database records JUVEDERM gel implants under P050047, while the current manufacturer page documents the US collection and hyaluronic-acid family context.

Limit: A family PMA record does not verify every catalogue variant, formulation, supplement, or non-US presentation.

JUVEDERM gel implants — PMA P050047About the Juvéderm filler collection

Catalogue relationship

Matched identities and variants

11 matches

Provenance

Sources checked for this profile

3 sources · checked 14 August 2026
  1. Manufacturer

    1. About the Juvéderm filler collection

    Allergan Aesthetics, an AbbVie company · United States

    Open source ↗

    Supports: Juvéderm family identity, named family context, and hyaluronic-acid material class.

  2. Regulator

    2. FDA-approved dermal fillers

    U.S. Food and Drug Administration · United States

    Open source ↗

    Supports: Regulatory-method context and the requirement to verify individual filler records and labels.

  3. Regulator

    3. JUVEDERM gel implants — PMA P050047

    U.S. Food and Drug Administration · United States

    Open source ↗

    Supports: The original US PMA family record, applicant identity, generic device class, and links to supplements and labeling.

Claim ledger

Every statement has a boundary

2 review claims
  1. 1

    Identity

    Juvéderm is a product-family identity with multiple separately named variants in the operational catalogue.

    Scope: Variants remain distinct records; the family page does not collapse their formulations or labels.

    Evidence: JUVEDERM gel implants — PMA P050047Evidence: About the Juvéderm filler collection
  2. 2

    Material / active name

    The cited US manufacturer material describes the Juvéderm collection as a hyaluronic-acid filler family.

    Scope: Family-level material class only; exact composition must be checked in variant-specific labeling.

    Evidence: About the Juvéderm filler collection

Use boundary

What this record does not establish

  • Regulatory statusOnly within a source's named jurisdiction; family-profile review does not establish status elsewhere.
  • Authenticity or supply chainA catalogue name cannot authenticate an individual box, lot, or seller.
  • Clinical suitabilityNo product selection, patient assessment, dose, protocol, or injection technique is provided.
  • Availability or equivalenceNames, formulations, units, and presentations can vary by market and over time.

Separate reference from record-keeping

Document the exact product and lot actually used

Aesthetic Pass records treatment identity, lot information, photos, and injection maps. The atlas itself never chooses a product or treatment.

Explore traceability