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MONALISAMONALISA Filler (Lidocaine)

MONALISA is a Hyaluronic acid filler product (Class III device), registered by Genoss Co.,Ltd.. Linked registrations: UK PARD-2657665, UK PARD-2657682, Australia 481247. Data as of 2026-11-09.

  • Regulatory classHyaluronic acid filler · Class III device
  • HolderGenoss Co.,Ltd.
  • JurisdictionsUK · AU
  • Updated2026-11-09 · v1

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

Registration and basics

MONALISA

Product
Regulatory class
Class III device
Category
Hyaluronic acid filler
UK · MHRA device registration (not an approval)
PARD-2657665
UK · MHRA device registration (not an approval)
PARD-2657682
Australia · TGA ARTG device
481247
Name on registration
MONALISA Filler
Registrant
Genoss Co. Ltd.
UK Responsible Person
Emergo Consulting (UK) Limited (UK Responsible Person)
Registered on
2022-02-01
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-2657665; 3 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. UK

    PARD-2657665 registered

  2. UK

    PARD-2657682 registered

  3. AU

    481247 ARTG start date

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

2
  • PARD-2657665: registered2022-02-01
  • PARD-2657682: registered2022-02-01

Sources

3