Medcxy

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

TeosyalTeosyal PureSense Ultra Deep

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Teosyal is a Hyaluronic acid filler product (Class III device), registered by Teoxane SA. Linked registrations: UK PARD-5636292, UK PARD-4721891, UK PARD-4721986 and 2 more. Data as of 2026-11-09.

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

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

Registration and basics

Teosyal

Product
Regulatory class
Class III device
Category
Hyaluronic acid filler
UK · MHRA device registration (not an approval)
PARD-5636292
UK · MHRA device registration (not an approval)
PARD-4721891
UK · MHRA device registration (not an approval)
PARD-4721986
UK · MHRA device registration (not an approval)
PARD-1882210
Australia · TGA ARTG device
235950
Name on registration
TEOSYAL® PureSense ULTRA DEEP
Registrant
Teoxane S.A.
UK Responsible Person
Emergo Consulting (UK) Limited （UK Responsible Person）
Registered on
2025-11-20
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-5636292; 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

    235950 ARTG start date

  2. UK

    PARD-4721891 registered

  3. UK

    PARD-4721986 registered

  4. UK

    PARD-5636292 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-5636292: registered2025-11-20
  • PARD-4721891: registered2024-07-13
  • PARD-4721986: registered2024-07-13

Sources

5