EVERYWAY4ALL

FDA Device Registration & Listing · Chino, CA, US · Registration 3011267903

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
3011267903
FEI Number
3011267903
Entity Name
EVERYWAY4ALL
City/State/Country
Chino, CA, US
Establishment Address
14636 CENTRAL AVE, Chino, CA 91710, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
EVERYWAY4ALL (Owner Number: 10053071)
Owner / Operator Contact Address
14636 CENTRAL AVE, Chino, CA 91710, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

EV-820 EM-5200 SG5075 KF4040 KF5050 SG7090 TKF5050

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2017-02-15
GXY Electrode, Cutaneous Neurology Class 2 882.1320 2016-12-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EVERYWAY4ALL
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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011267903. Last updated year: 2026. Please use registration number 3011267903 when referencing this establishment in official correspondence.
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