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VIRTUSENSE TECHNOLOGIES, INC.

US

Last updated May 30, 2026

What VIRTUSENSE TECHNOLOGIES, INC. makes

Virtusense Technologies, Inc. manufactures virtual-display rehabilitation systems designed for clinical use, focusing on non-supportive balance and mobility training. Their primary product, VSTBalance, provides interactive virtual reality-based exercises to support physical therapy and rehabilitation programs.

The company’s portfolio is regulated under Class II medical devices in the United States and is listed in the FDA’s Unique Device Identifier (UDI) database. Virtusense Technologies, Inc. is based in the US.

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 Virtusense Technologies, Inc. manufacture?

Virtusense Technologies, Inc. specializes in virtual-display rehabilitation systems for clinical use, specifically non-supportive devices. Their primary focus is on balance and mobility training, with products like the VSTBalance designed to provide interactive virtual reality-based exercises. These devices are intended to support physical therapy and rehabilitation programs by offering immersive, guided training environments.

Where is Virtusense Technologies, Inc. based?

Virtusense Technologies, Inc. is headquartered in the United States. The company’s location is relevant for regulatory compliance and device distribution, as it operates within the FDA’s jurisdiction for medical device authorization.

Which regulatory registries list Virtusense Technologies, Inc.’s devices?

Virtusense Technologies, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for authorized medical devices, allowing healthcare providers and regulators to verify product details and compliance status.

How are Virtusense Technologies, Inc.’s devices classified under US regulations?

Virtusense Technologies, Inc.’s devices fall under Class II classification in the United States. This classification is assigned based on the risk level of the device, where Class II devices require special controls in addition to general controls to ensure safety and effectiveness, such as those used in virtual-display rehabilitation systems like VSTBalance.

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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EUDAMED SRN
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FDA FEI Number
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DUNS Number
117239864

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
VSTBalance v2024-01Jan-11-e940.json
FDA UDI
Class IIActive

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