Virtusense Technologies, Inc.
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Virtusense Technologies, Inc. is a medical device manufacturer, with 3 devices listed in FDA GUDID (FDA Class II) as of 14 Nov 2026.
- Devices
- 3
Registry facts
- Registries
- FDA GUDID 3
- Device classes
- FDA Class II 3
- Identifiers
- DUNS 117239864
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.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 117239864
Frequently asked questions
How many devices does VIRTUSENSE TECHNOLOGIES, INC. have in the registry?
The registry currently lists 3 devices for VIRTUSENSE TECHNOLOGIES, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list VIRTUSENSE TECHNOLOGIES, INC.'s devices?
Among its 3 most recently registered devices, VIRTUSENSE TECHNOLOGIES, INC. has devices listed in FDA GUDID (3 devices).
What risk classes do VIRTUSENSE TECHNOLOGIES, INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for VIRTUSENSE TECHNOLOGIES, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from VIRTUSENSE TECHNOLOGIES, INC. in the registry?
The most recently registered devices listed for VIRTUSENSE TECHNOLOGIES, INC. include Proactive Strides 1.0.7, Proactive You 1.0.3 and VSTBalance v2024-01Jan-11-e940.json.