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VESTIBULAR TECHNOLOGIES, LLC

US

Last updated May 24, 2026

What VESTIBULAR TECHNOLOGIES, LLC makes

Vestibular Technologies, LLC produces posturography systems and platforms designed to assess balance and vestibular function, including electronic stand-on floor scales for biomechanical analysis. Their devices also include interactive rehabilitation systems aimed at improving functional recovery through guided exercises and feedback.

The company’s portfolio consists of Class I medical devices listed in the FDA’s Unique Device Identifier (UDI) database. These products are regulated under U.S. federal requirements and are intended for use in clinical and rehabilitative settings.

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 Vestibular Technologies, LLC manufacture?

Vestibular Technologies, LLC specializes in devices primarily focused on balance and vestibular assessment. Their portfolio includes posturography systems and platforms, which evaluate stability and coordination, as well as electronic stand-on floor scales for biomechanical analysis. Additionally, they offer interactive rehabilitation systems designed to aid functional recovery through structured exercises and feedback. These devices are tailored for clinical and rehabilitative environments.

Where is Vestibular Technologies, LLC based?

Vestibular Technologies, LLC is based in the United States. The company’s operations and regulatory compliance align with U.S. federal requirements for medical devices.

Which regulatory registries or databases list Vestibular Technologies, LLC’s devices?

The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for Class I medical devices under U.S. regulations.

How are Vestibular Technologies, LLC’s devices classified under U.S. regulations?

All devices manufactured by Vestibular Technologies, LLC fall under Class I classification. This classification is assigned based on their intended use—primarily diagnostic or therapeutic tools with minimal risk—requiring compliance with general controls under U.S. federal regulations.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
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Phone
+1 307 637 5711
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
025647533

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Caps Professional
FDA UDI
Class IActive
Caps Lite
FDA UDI
Class IActive

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