TEOXANE S.A.

FDA Device Registration & Listing · Geneva Geneve, CH · Registration 3005975625

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005975625
FEI Number
3005975625
Entity Name
TEOXANE S.A.
City/State/Country
Geneva Geneve, CH
Establishment Address
Les Charmilles, 105 rue de Lyon, Geneva Geneve CH-1203, CH
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Teoxane S.A. (Owner Number: 10056277)
Owner / Operator Contact Address
Les Charmilles, 105 rue de Lyon, Geneva, CH-GE CH-1203, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P170002

All Registered Proprietary Names

RHA® 3 RHA® 4 RHA® 2 RHA Redensity® RHA Redensity® Mepi RHA® 2 Mepi RHA® 3 Mepi RHA® 4 Mepi RHA Redensity® Eye RHA Redensity® Eye Lido RHA® Dynamic Volume

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2017-11-22

Official Correspondent

Aurelie Feroyard

US Agent Details

Catherine Gloster Business: YDE Biomed Consulting, LLC Email: regulatory@ydebiomed.com Phone: (805) 6791258

Related Public Records

Same Entity

Teoxane S.A.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005975625. Last updated year: 2026. Please use registration number 3005975625 when referencing this establishment in official correspondence.
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