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Evoke Neuroscience, Inc.

US

Last updated May 30, 2026

What Evoke Neuroscience, Inc. makes

Evoke Neuroscience, Inc. manufactures electroencephalograph systems designed for monitoring brain activity, including the eVox System. These devices are intended for clinical use in recording and analyzing electrical signals from the brain, aiding in diagnostic and research applications.

The company’s portfolio is classified under FDA Class II devices and is authorised through 510(k) and UDI registrations in the United States. The systems are listed in the FDA’s regulatory databases, adhering to U.S. medical device compliance requirements.

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 Evoke Neuroscience, Inc. manufacture?

Evoke Neuroscience, Inc. specializes in electroencephalograph systems, which are devices used to monitor brain activity by recording electrical signals. Their primary product, the eVox System, is designed for clinical applications in diagnosing and researching neurological conditions.

Where is Evoke Neuroscience, Inc. based?

Evoke Neuroscience, Inc. is headquartered in the United States. The company’s devices are developed and authorised in compliance with U.S. regulatory standards.

Which regulatory registries list Evoke Neuroscience’s devices?

Evoke Neuroscience’s devices are listed in the FDA’s 510(k) premarket notification database and the FDA’s Unique Device Identifier (UDI) system. These registries ensure compliance with U.S. medical device regulations.

How are Evoke Neuroscience’s devices classified by regulatory authorities?

Evoke Neuroscience’s devices fall under FDA Class II classification, which applies to moderate-risk medical products requiring special controls to ensure safety and effectiveness before market authorisation.

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

Information

Country
US
Address
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LinkedIn
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Facebook
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Phone
9172616096
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
962456898

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
eVox System EVO-002-400-000
FDA UDI
Class IIActive
eVox System K171781
FDA 510(k)
Class IIActive

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