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Revanesse ShapeRevanesse Shape+

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Revanesse Shape is a Skin booster product (Class III device), registered by Prollenium Medical Technologies Inc.. Linked registrations: EU B-PN40094QE, EU B-PN40095QG, EU B-PN40096QJ and 5 more. Data as of 2026-11-09.

  • Regulatory classSkin booster · Class III device
  • HolderProllenium Medical Technologies Inc.
  • JurisdictionsEU · UK · AU
  • Updated2026-11-09 · v1

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

Registration and basics

Revanesse Shape

Product
Regulatory class
Class III device
Category
Skin booster
EU · EUDAMED device record
B-PN40094QE
EU · EUDAMED device record
B-PN40095QG
EU · EUDAMED device record
B-PN40096QJ
EU · EUDAMED device record
B-PN40116PX
UK · MHRA device registration (not an approval)
PARD-3315765
UK · MHRA device registration (not an approval)
PARD-3283628
UK · MHRA device registration (not an approval)
PARD-2146007
UK · MHRA device registration (not an approval)
PARD-2146015
Other registrations
2 more, see the timeline
Name on registration
Revanesse® Shape + with Lidocaine 1.0 mL
Registrant
Prollenium Medical Technologies Inc.
EU authorised representative
Emergo Europe B.V.（NL-AR-000000116）
First approval
Not obtained from an official source
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 B-PN40094QE; 10 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-2146007 registered

  2. UK

    PARD-2146015 registered

  3. UK

    PARD-2146032 registered

  4. UK

    PARD-3283628 registered

  5. UK

    PARD-3315765 registered

  6. AU

    450108 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

5
  • PARD-3315765: registered2022-07-19
  • PARD-3283628: registered2022-07-01
  • PARD-2146007: registered2021-12-02
  • PARD-2146015: registered2021-12-02
  • PARD-2146032: registered2021-12-02

Sources

10