NEXALIN TECHNOLOGY, INC.

FDA Device Registration & Listing · Houston, TX, US · Registration 3014498660

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014498660
FEI Number
3014498660
Entity Name
NEXALIN TECHNOLOGY, INC.
City/State/Country
Houston, TX, US
Establishment Address
1776 Yorktown, Ste 550, Houston, TX 77056, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Nexalin Technology, Inc. (Owner Number: 10057669)
Owner / Operator Contact Address
1776 Yorktown, Ste 550, Houston, TX 77056, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K024377
PMA Number
N/A

All Registered Proprietary Names

Nexalin ADI Patient Cable Electrode Set

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QJQ Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety Neurology Class 2 882.5800 2018-05-10

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nexalin Technology, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014498660. Last updated year: 2026. Please use registration number 3014498660 when referencing this establishment in official correspondence.
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