Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2022388

FEI Number

2022388

Entity Name

THE ELECTRODE STORE

City/State/Country

Buckley, WA, US

Establishment Address

159 W Mason Avenue, Buckley, WA 98321, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

The Electrode Store (Owner Number: 10025712)

Owner / Operator Contact Address

159 W Mason Avenue, Buckley, WA 98321, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Electrode Store, Alera TES, DPNCheck The Electrode Store Alera TES ECG Electrodes, Multi-Function SURESET DPNCHECK ALERA TES ADVANCE ELECTRODE STORE NC-STAT Protectrode Sterile Intraoperative Electrodes The Electrode Store Subdermal Needle Electrodes Alera TES ECG Electrodes Alera TES Concentric Needle Electrode The Electrode Store Disposable EEG Hydrogel Electrodes

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GXY	Electrode, Cutaneous	Neurology	Class 2	882.1320	2025-07-01
GXY	Electrode, Cutaneous	Neurology	Class 2	882.1320	2008-05-01
MLN	Electrode, Electrocardiograph, Multi-Function	Cardiovascular	Class 2	870.2360	2024-08-10
KMK	Device, Intravascular Catheter Securement	General Hospital	Class 1	880.5210	2024-08-05
JXE	Device, Nerve Conduction Velocity Measurement	Neurology	Class 2	882.1550	2025-07-01
GXZ	Electrode, Needle	Neurology	Class 2	882.1350	2008-05-01
GXY	Electrode, Cutaneous	Neurology	Class 2	882.1320	2009-12-10
GXZ	Electrode, Needle	Neurology	Class 2	882.1350	2008-05-01
DRX	Electrode, Electrocardiograph	Cardiovascular	Class 2	870.2360	2024-08-05
IKT	Electrode, Needle, Diagnostic Electromyograph	Physical Medicine	Class 2	890.1385	2008-05-01
GXY	Electrode, Cutaneous	Neurology	Class 2	882.1320	2024-08-05

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Electrode Store

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
9616086	DJ ORTHOPEDICS DE MEXICO, S.A. DE C.V.	TIJUANA Baja California, MX

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2022388. Last updated year: 2026. Please use registration number 2022388 when referencing this establishment in official correspondence.