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VIRTUALIS

US

Last updated May 23, 2026

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.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Virtualis manufacture?

Virtualis specializes in software and systems for biomechanical function analysis and posturography. Their devices include virtual reality-based rehabilitation tools, such as the DVA VR and Motorway Simulation, as well as posturography platforms like the Sway Referenced Visual Environment. These tools are designed for assessing and improving motor coordination, balance, visual adaptation, and specific physiological functions like eye-hand coordination and spinal mobility.

Where is Virtualis based, and how does that affect its devices?

Virtualis is based in the United States, where its devices are regulated under applicable FDA standards. Since the company operates within the US, its products fall under FDA oversight, including classification under Class I (generally low-risk) and Class II (moderate-risk) categories, depending on their intended use and potential risks.

Are Virtualis’s devices listed in any regulatory registries?

Yes, Virtualis’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the US, ensuring transparency and traceability for healthcare providers and regulators.

How are Virtualis’s devices classified by the FDA?

Virtualis’s devices are classified under FDA’s Class I (for low-risk items like some rehabilitation software) and Class II (for moderate-risk items like posturography systems). Classification depends on factors like the device’s purpose, potential risks, and intended use—such as assessing balance or motor function—rather than the company itself.

What distinguishes Virtualis’s posturography and biomechanical analysis tools from other solutions?

Virtualis’s tools leverage virtual reality (VR) and simulation platforms to create immersive environments for rehabilitation and assessment. For example, devices like SpineVR or StroopVR combine VR with biomechanical metrics to evaluate and train specific functions—such as spinal mobility or cognitive-motor coordination—unlike traditional non-VR systems that may rely solely on static measurements or physical equipment.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
267153884

Catalogue (63)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
Dva Vr V1.2.10
FDA UDI
Class IIActive
Motorway Simulation v2.3.4
FDA UDI
Class IIActive
Sway Referenced Visual Environment V2.3.4
FDA UDI
Class IIActive
AirRaceVR v1.3.3
FDA UDI
Class IIActive
SpineRotationVR V1.1.5
FDA UDI
Class IIActive
StroopVR V0.1.8
FDA UDI
Class IIActive
SpineVR v1.0.1
FDA UDI
Class IIActive
Dynamic Subjective Visual Vertical V2.3.4
FDA UDI
Class IIActive
Head-Eye-Coordination V1.2.7
FDA UDI
Class IIActive
Adaptation Test v1.3.1
FDA UDI
Class IIActive
Whac-a-Mush V1.1.2
FDA UDI
Class IIActive
Optical Flow v3.4.10
FDA UDI
Class IIActive
WalkVR V0.0.16
FDA UDI
Class IIActive
Ctsib Vr v1.2.0
FDA UDI
Class IIActive
Cervicocephalic Relocation Test V2.3.4
FDA UDI
Class IIActive
Upper Limb ROM v1.4.3
FDA UDI
Class IIActive
RelaxationVR V1.0.5
FDA UDI
Class IIActive
BirdVR v1.3.5
FDA UDI
Class IIActive
Reading (Sway Referenced) v1.2.9
FDA UDI
Class IIActive
Weight Bearing v1.0.24
FDA UDI
Class IIActive
Spatial Navigation V1.5.8
FDA UDI
Class IIActive
Bells Test VR v2.1.0
FDA UDI
Class IIActive
Subjective Visual Vertical V2.3.4
FDA UDI
Class IIActive
Mirror Lower Limb v1.0.18
FDA UDI
Class IIActive
Unilateral Stance v1.1.6
FDA UDI
Class IIActive
MotionVR Research V0.2.1
FDA UDI
Class IIActive
Sot V1.2.0
FDA UDI
Class IIActive
LOS Rehab v1.1.5
FDA UDI
Class IIActive
PhysioVR v1.0
FDA UDI
Class IIActive
Mirror & Ball v1.0.1
FDA UDI
Class IIActive
EscalatorVR V1.1.0
FDA UDI
Class IIActive
CrowdVR v1.3.2
FDA UDI
Class IIActive
Car Simulation v1.2.9
FDA UDI
Class IIActive
StaticVR V1
FDA UDI
Class IActive
Electrical Track V0.6.1
FDA UDI
Class IIActive
RotationVR v0.3.2
FDA UDI
Class IIActive
SquatVR V2.1.4
FDA UDI
Class IIActive
hCTSIB VR V1.2.0
FDA UDI
Class IIActive
Sea Simulation v1.2.9
FDA UDI
Class IIActive
Motor Control Test V0.9.0
FDA UDI
Class IIActive
MotionProgram v1.1.0
FDA UDI
Class IIActive
Supermarket v1.5.8
FDA UDI
Class IIActive
Lift v1.2.9
FDA UDI
Class IIActive
ReflexVR V1.3.10
FDA UDI
Class IIActive
Weight Repartition V1.1.2
FDA UDI
Class IIActive
Target Tracking V2.3.4
FDA UDI
Class IIActive
Poursuit CoP v1.2.7
FDA UDI
Class IIActive
HemiNeglect v1.3.7
FDA UDI
Class IIActive
BalanceVR v1.0
FDA UDI
Class IIActive
Waves (sway Referenced) V1.2.9
FDA UDI
Class IIActive

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Virtualis Montpellier Herault · FR FEI 3014873207