Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004786509

FEI Number

3004786509

Entity Name

InterX Technologies

City/State/Country

Plano, TX, US

Establishment Address

3465 Technology Dr., Suite A, Plano, TX 75074, US

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device

Owner / Operator

InterX Technologies (Owner Number: 10051305)

Owner / Operator Contact Address

3465 Technology Dr., Suite A, Plano, TX 75074, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K053626

PMA Number

N/A

All Registered Proprietary Names

InterX Self-Adhesive Dual Electrode - Non-Sterile InterX5000 InterX500 Flexible Array Electrode

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GXY	Electrode, Cutaneous	Neurology	Class 2	882.1320	2016-03-01
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2016-03-01
GXY	Electrode, Cutaneous	Neurology	Class 2	882.1320	2016-03-01

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

InterX Technologies

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K070612	Top-Rank Health Care Equipment Co., Ltd.	TOP-RANK ADHESIVE ELECTRODE	2007-05-07
K123915	Grass Technologies, an Astro-Med, Inc. Product Gro	DE48-PLUS	2013-04-24
K073532	Technomed Europe	DISPOSABLE ADHESIVE SURFACE ELECTRODES, DISC ELECTRODES	2008-05-01
K260363	Ceribell, Inc.	Ceribell Brain Monitor Headband	2026-04-03
K091762	Covidien	DURA-STICK SELF-ADHESIVE ELECTRODES WITH ALOE	2009-12-22

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3005581220	SPES MEDICA S.P.A	BATTIPAGLIA Salerno, IT
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004786509. Last updated year: 2026. Please use registration number 3004786509 when referencing this establishment in official correspondence.