Virtualis
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Virtualis is a medical device manufacturer, with 63 devices listed in FDA GUDID (FDA Class II and I) as of 13 Nov 2026.
- Devices
- 63
Registry facts
- Registries
- FDA GUDID 63
- Device classes
- FDA Class II 61
- FDA Class I 2
- Sites and related companies
- Virtualis France
- Identifiers
- DUNS 267153884
What Virtualis makes
Virtualis develops software and systems for biomechanical function analysis and posturography, including virtual reality-based rehabilitation tools and simulation platforms. Their portfolio includes applications like virtual reality environments for motor coordination, visual adaptation testing, and balance assessment, as well as games and exercises targeting specific physiological functions such as eye-hand coordination and spinal mobility.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Virtualis operates from the United States, where these products are regulated under applicable medical device standards.
Catalogue
Search and filter all 63 devicesShowing 1-50 of 63
Company details
- DUNS number
- 267153884
Sites
- Virtualis FRFEI 3014873207 0 devices
Frequently asked questions
How many devices does VIRTUALIS have in the registry?
The registry currently lists 63 devices for VIRTUALIS. Devices recorded under merged duplicate company entries are counted once.
Which registries list VIRTUALIS's devices?
Among its 50 most recently registered devices, VIRTUALIS has devices listed in FDA GUDID (50 devices).
What risk classes do VIRTUALIS's devices fall under?
Among its 50 most recently registered devices, the classes recorded for VIRTUALIS's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from VIRTUALIS in the registry?
The most recently registered devices listed for VIRTUALIS include DVA VR V1.2.10, Motorway Simulation v2.3.4, Sway Referenced Visual Environment V2.3.4 and AirRaceVR v1.3.3.