LUMEEN
France FR-MF-000022236 Last updated 21 Oct 2026
- Devices
- 19
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Système Lumeen v3 Ref 6C-V03
Dispositif 4 casques Ref 4C-V04
Lumeen Manager Ref DOPlatform
Lumeen Ref Lumeen-v3
Système Lumeen v3 Ref 2C-V03
Système Lumeen v2 Ref 3C-V02
Dispositif 6 casques Ref 6C-V04
Système Lumeen v3 Ref 1C-V03
Dispositif 2 casques Ref 2C-V04
Système Lumeen v3 Ref 3C-V03
Dispositif 5 casques Ref 5C-V04
Système Lumeen v2 Ref 6C-V02
Lumeen Ref Lumeen-v4 module Evasion
Système Lumeen v3 Ref 1CH-V03
Lumeen Ref Lumeen-v4 module Relaxation
Système Lumeen v2 Ref 1C-V02
Lumeen Ref Lumeen-v2
Dispositif 3 casques Ref 3C-V04
Dispositif 1 casque hôpital Ref 1CH-V04
About
Virtual social and therapeutic reality for the elderly, sick and disabled.
What LUMEEN makes
The company manufactures headset-based systems designed for therapeutic and social virtual reality applications, including configurations with two, three, four, five, and six headsets. These systems are intended for use with elderly individuals, patients, and people with disabilities, enabling immersive experiences for rehabilitation, cognitive stimulation, or social interaction. The portfolio includes standalone headset devices and multi-user setups, alongside software management tools for coordinating sessions.
All listed devices fall under Class I classification in the EU and are registered in the EUDAMED database. The company is based in France and adheres to EU Medical Device Regulation (MDR) requirements for Class I products, ensuring compliance with mandatory registration and traceability standards.
Information
- Country
- France
- Address
- 58, Avenue Debourg, LYON, France
- Website
- www.lumeen.com
- linkedin.com/company/lumeen
- facebook.com/lumeenFR
- [email protected]
- EUDAMED SRN
- FR-MF-000022236