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Nexalin Technology, Inc.

Active in EUDAMED

United Statesfrom EUDAMED address EUDAMED FDA SRN US-MF-000058289 FEI 3014498660

Devices
3
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

What Nexalin Technology, Inc. makes

Nexalin Technology, Inc. manufactures a transcranial electrical stimulation system designed for professional use, delivering continuous-current waveforms to target midbrain regions. The device is intended to support neurochemical normalization in the brain, addressing conditions such as anxiety and insomnia without medication.

The company’s transcranial electrical stimulation system is classified as a Class III medical device and is listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

Company details

EUDAMED SRN
US-MF-000058289
FDA FEI number
3014498660
EUDAMED status
Active
EUDAMED registered name
Nexalin Technology, Inc.
EUDAMED abbreviated name
NXL
Address
1776 Yorktown, Ste 550, Houston, TX, 77056
Website
nexalin.com/
Phone
+1-8322600222
PRRC contact
Carolyn Shelton(public in EUDAMED)

From the company website

Read 18 Oct 2026

Scientific research now confirms that anxiety and insomnia can be caused by irregularities in the brain’s neurochemicals. Through our patented, frequency-related, advanced waveform that interacts with the deep centers of the midbrain, our Nexalin device supports the normalization of these chemicals. And best of all, without medication.

From the manufacturer's own website. Source

Frequently asked questions

How many devices does Nexalin Technology, Inc. have in the registry?

The registry currently lists 3 devices for Nexalin Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Nexalin Technology, Inc.'s devices?

Among its 3 most recently registered devices, Nexalin Technology, Inc. has devices listed in FDA GUDID (3 devices).

What risk classes do Nexalin Technology, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Nexalin Technology, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Nexalin Technology, Inc. in the registry?

The most recently registered devices listed for Nexalin Technology, Inc. include Nexalin ADI DXD 0080, Nexalin KS02000 and Nexalin KS02001.

Generated automatically from registry data and not verified by a human reviewer.