Product dossierBuilt from registrations, label text and platform-curated data
Teosyal RHA 3RHA3
Teosyal RHA 3 is a Hyaluronic acid filler product (Class III device), registered by Teoxane SA. Linked registrations: UK PARD-5636297, UK PARD-5526443, UK PARD-5526450 and 5 more. First approved in US on 2017-10-19 (P170002). Data as of 2026-11-09.
- Regulatory classHyaluronic acid filler · Class III device
- HolderTeoxane SA
- JurisdictionsUS · UK · AU
- Updated2026-11-09 · v1
Registration and basics are public; findings and prices need an account
Registration and basics
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
- AU
294482 ARTG start date
- US
P170002 first approved
- UK
PARD-4721919 registered
- UK
PARD-4721989 registered
- UK
PARD-5526443 registered
- UK
PARD-5526450 registered
- UK
PARD-5636297 registered
- US
P170002 · P170002/S041
Real-Time Process|Process Change - Manufacturer/Sterilizer/Packager/Supplier|Approval for implementation of parametric release after termina…
- AU
526254 ARTG start date
- US
P170002 · P170002/S050
Panel Track|Change Design/Components/Specifications/Material|Approval for RHA Redensity® Eye Lido and RHA Redensity® Eye for expanding the i…
- US
P170002 · P170002/S052
Normal 180 Day Track No User Fee|Labeling Change - PAS|Approval for the final labeling of RHA® Redensity Mepi. This follows the completion o…
- US
P170002 · P170002/S055
Real-Time Process|Labeling Change - Indications/instructions/shelf life/tradename|approval for updating the labeling of RHA®3 Mepi to a new …
- US
P170002 · P170002/S058
30-Day Notice|Process Change - Manufacturer/Sterilizer/Packager/Supplier|Approval for the replacement of glass crystallizers with Stainless …
- US
P170002 · P170002/S059
30-Day Notice|Process Change - Manufacturer/Sterilizer/Packager/Supplier|Approval for an alternative qualified laboratory for Biological Ind…
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.
Cross findings · Price observations
Recent changes
5- P170002: 30-Day Notice|Process Change - Manufacturer/Sterilizer/Packager/Supplier|Approva…2026-08-31
- P170002: 30-Day Notice|Process Change - Manufacturer/Sterilizer/Packager/Supplier|Approva…2026-08-28
- P170002: Real-Time Process|Labeling Change - Indications/instructions/shelf life/tradenam…2026-07-27
- P170002: Normal 180 Day Track No User Fee|Labeling Change - PAS|Approval for the final la…2026-07-02
- P170002: Panel Track|Change Design/Components/Specifications/Material|Approval for RHA Re…2026-05-12