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REVOLAX Sub-QREVOLAX SUB-Q with Lidocaine

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REVOLAX Sub-Q is a Hyaluronic acid filler product (Class III device), registered by ACROSS CO., LTD.. Linked registrations: Australia 509129. Data as of 2026-11-09.

  • Regulatory classHyaluronic acid filler · Class III device
  • HolderACROSS CO., LTD.
  • JurisdictionsAU
  • Updated2026-11-09 · v1

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

Registration and basics

REVOLAX Sub-Q

Product
Regulatory class
Class III device
Category
Hyaluronic acid filler
Australia · TGA ARTG device
509129
Name on registration
REVOLAX™ SUB-Q with Lidocaine
Registrant
Hugel Australia Pty Ltd
Manufacturer
Across Co Ltd
ARTG start date
2025-08-15
Models and sizes
Nil variant (as 1 device) Needle gauge: 25Gx1/2"
Checked against official page
2026-11-09

Public: fields from the registration record.This product record is still pending review.

Label facts by jurisdiction

What each jurisdiction's label says for the same attribute; gaps are marked Not reported, irrelevant ones N/A

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Registration timeline

  1. AU

    509129 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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    Sources

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