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Product dossierBuilt from registrations, label text and platform-curated data

Stylage SStylage S Lidocaine

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Stylage S is a Hyaluronic acid filler product (Class III device), registered by Laboratoires VIVACY. Linked registrations: UK PARD-757844, UK PARD-757850, UK PARD-757858 and 2 more. Data as of 2026-11-09.

  • Regulatory classHyaluronic acid filler · Class III device
  • HolderLaboratoires VIVACY
  • JurisdictionsUK · AU
  • Updated2026-11-09 · v1

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

Registration and basics

Stylage S

Product
Regulatory class
Class III device
Category
Hyaluronic acid filler
UK · MHRA device registration (not an approval)
PARD-757844
UK · MHRA device registration (not an approval)
PARD-757850
UK · MHRA device registration (not an approval)
PARD-757858
Australia · TGA ARTG device
292899
Australia · TGA ARTG device
292901
Name on registration
STYLAGE® S Mepivacaine
Registrant
Laboratoires VIVACY
UK Responsible Person
VIVACY LABORATOIRES LTD（UK Responsible Person）
Registered on
2021-04-21
Models and sizes
General Medical Device; Class III
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 PARD-757844; 5 registrations linked.

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. AU

    292899 ARTG start date

  2. AU

    292901 ARTG start date

  3. UK

    PARD-757844 registered

  4. UK

    PARD-757850 registered

  5. UK

    PARD-757858 registered

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

3
  • PARD-757844: registered2021-04-21
  • PARD-757850: registered2021-04-21
  • PARD-757858: registered2021-04-21

Sources

5