Teoxane S.A.
Country not established FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Teoxane S.A. makes
Teoxane S.A. makes dermal fillers, including products such as RHA 2, RHA 3, and RHA 4. These are specific types of injectable implants used for various cosmetic and medical applications.
The company's portfolio is regulated as Class III devices and is listed in the FDA's PMA registry. The company is based in the US, where its products are subject to regulatory oversight by the FDA. The devices are required to meet specific safety and efficacy standards prior to approval and listing.
Catalogue
Rha 2, Rha 3, Rha 4 Ref P170002
Regimes: PMA Registry: PMA
FDA establishments
- Teoxane S.A. Geneva Geneve · CH FEI 3005975625
Frequently asked questions
How many devices does Teoxane S.A. have in the registry?
The registry currently lists 1 device for Teoxane S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Teoxane S.A.'s devices?
Among its 1 most recently registered device, Teoxane S.A. has devices listed in FDA PMA (1 device).
What risk classes do Teoxane S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Teoxane S.A.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Teoxane S.A. in the registry?
The most recently registered devices listed for Teoxane S.A. include RHA 2, RHA 3, RHA 4.
Which FDA establishments are linked to Teoxane S.A.?
1 FDA establishment is linked to Teoxane S.A. in the registry; they are listed on the company page.