Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8022189

FEI Number

3004668996

Entity Name

C.M.P. CANADIAN MEDICAL PRODUCTS INC.

City/State/Country

Aurora Ontario, CA

Establishment Address

212 Earl Stewart Drive, Unit 6, Aurora Ontario L4G6V7, CA

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

CMP CANADIAN MEDICAL PRODUCTS INC. (Owner Number: 8022189)

Owner / Operator Contact Address

7-10 Furbacher Ln, --, Aurora, CA-ON L4G6W1, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K091236

PMA Number

N/A

All Registered Proprietary Names

PROCARBON IFC ELECTRODES Sponges CMP Vacuum Leadwires Vacuum Suction Cups Stereo Solution CMP CABLES Mono-DIN Adaptor Stereo-DIN Adaptor Mono Solution Tuchel-DIN Adaptor Pro Carbon Electrodes Pro Carbon ProEnduro PROFLEX ELECTRODES Pro Flex + AgF Pro Flex AgC ProVerta Pro Flex CC CMP Neuropulse Combo

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LIH	Interferential Current Therapy	Neurology	Class 2	882.5890	2013-03-22
IPF	Stimulator, Muscle, Powered	Physical Medicine	Class 2	890.5850	2013-03-22
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2013-03-22
IPF	Stimulator, Muscle, Powered	Physical Medicine	Class 2	890.5850	2008-10-30
IKD	Cable, Electrode	Physical Medicine	Class 2	890.1175	1999-05-20
GXY	Electrode, Cutaneous	Neurology	Class 2	882.1320	2008-10-30
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2012-09-13
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2011-09-26

Official Correspondent

Riccardo Dente

US Agent Details

Lilian Llull Business: TechLink International, LLC Email: lilian@techlinkusa.net Phone: (305) 3770077

Related Public Records

Same Entity

CMP CANADIAN MEDICAL PRODUCTS INC.

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
K030403	Cefar Medical AB	CEFAR REHAB 2 AND REHAB 2 PRO	2003-07-17
K231440	Shenzhen Roundwhale Technology Co. , Ltd.	Combo Electrotherapy Device	2023-11-03
K820884	Nitron Electronics	ELECTRICAL MUSCLE STIMULATOR	1982-04-29
K201958	Therasigma, LLC	ETD Family of Electrotherapy Devices	2020-08-04
K964028	Mettler Electronics Corp.	SYS STIM 226	1997-02-03

Similar Registrations

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3012316249	COMPASS HEALTH BRANDS (CORPORATE OFFICE)	Middleburg Heights, OH, US
3010805941	BIO PROTECH YANTAI INC	Yantai Shandong, CN
3004558433	BIOWAVE CORPORATION	NORWALK, CT, US
3014315574	BRH MEDICAL LTD	Jerusalem, IL
9615033	FUJI DYNAMICS LIMITED	Dongguan Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8022189. Last updated year: 2026. Please use registration number 8022189 when referencing this establishment in official correspondence.