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Galderma

Galderma is a global dermatology company and the principal brand and commercial context for Sculptra in Injectable Index. Galderma should not automatically be described as every product-level manufacturer or approval holder: FDA records identify Q-Med AB as the Sculptra applicant, while local labels can assign additional legal roles.

FieldGalderma
Injectable Index relationshipCommercial brand context for Sculptra
HeadquartersZug, Switzerland
Public statusListed on the SIX Swiss Exchange
TickerGALD
First trading dateMarch 22, 2024
Relevant business categoryInjectable Aesthetics

Galderma’s investor site confirms that Galderma Group AG shares have traded on the SIX Swiss Exchange under GALD since March 22, 2024 (Galderma share information 🔗). The company lists its headquarters in Zug, Switzerland (Galderma contact information 🔗).

ProductBrand and commercial companyDeveloper or originLegal manufacturerRegulatory applicant or approval holder
SculptraGaldermaProduct history predates the current Galderma public-company structureVerify from the applicable IFUQ-Med AB is the FDA PMA applicant

This matrix prevents four roles from being flattened into “made by Galderma.”

Galderma’s global Sculptra page establishes the current brand relationship (Galderma Sculptra 🔗). The FDA PMA database identifies Q-Med AB as applicant for Sculptra records (FDA PMA history 🔗).

Galderma controls the current global commercial narrative, product education, and much of the accessible official product documentation for Sculptra. Its role is especially relevant for:

  • current international IFU access
  • formulation and preparation updates
  • country launches and availability
  • new indication or certification announcements
  • portfolio and market context

These sources are authoritative for company position and product instructions when the document applies to the market being described. Promotional claims still need independent or regulatory support before becoming comparative clinical conclusions.

Sculptra’s regulatory identity is regional. A Galderma global announcement can establish a launch or company milestone, but it should not replace:

  • FDA approval records for the United States
  • a current regional IFU
  • the applicable legal manufacturer
  • the local approval holder
  • local indication and contraindication wording

Galderma’s 2025 annual report states that Sculptra launched in China and received European certification for expanded body indications during 2025 (Galderma 2025 annual report 🔗). Those are distinct regional developments, not a universal change in the Sculptra label.

DateEventWhy it changes interpretation
March 22, 2024Galderma Group AG began trading on SIX under GALDEstablishes current public-company status
2025Sculptra launched in ChinaExpands the product’s regional commercial context
2025Galderma reported European certification for expanded Sculptra body indicationsAdds a regional regulatory milestone without changing other markets automatically
2026Galderma continued global Sculptra positioning and published current product materialConfirms the brand remains a core injectable-aesthetics franchise

Do not use Galderma’s portfolio ownership to infer:

  • one global Sculptra indication
  • one legal manufacturer
  • identical preparation in every market
  • FDA approval for body use
  • clinical superiority over another PLLA product
  • Regional regulation separates Q-Med’s US applicant role from EU certification and Korean product information.
  • Sculptra contains the product-level composition, preparation, and approval context.
  • PLLA places Sculptra in its material family.
  • Sinclair provides the nearest initial company comparison through Lanluma.
  • Collagen Stimulators maps the full reference cluster.