Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029939996

FEI Number

3029939996

Entity Name

CHEK MEDICAL

City/State/Country

Aurora, CO, US

Establishment Address

25489 E Fair Dr, Aurora, CO 80016, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

CHEK Medical (Owner Number: 10089240)

Owner / Operator Contact Address

P.O. Box 462151, Aurora, CO 80046, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K200177

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

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	2023-11-25
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2023-11-25

Official Correspondent

Ke Zhao

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CHEK Medical

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
K221200	Xbody Hungary Kft.	XBody Go USA, XBody Pro USA	2023-01-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029939996. Last updated year: 2026. Please use registration number 3029939996 when referencing this establishment in official correspondence.