Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003782614

FEI Number

3003782614

Entity Name

CHIN KOU MEDICAL INSTRUMENT CO.,LTD.

City/State/Country

NEW TAIPEI CITY, TW

Establishment Address

2ND FL., NO. 68, SECTION 2, GUO DAO RD., LUZHOU DISTRICT,, NEW TAIPEI CITY 247, TW

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CHIN KOU MEDICAL INSTRUMENT CO.,LTD. (Owner Number: 9011147)

Owner / Operator Contact Address

2ND FL., NO. 68, SECTION 2, GUO DAO RD., LUZHOU DISTRICT, NEW TAIPEI CITY, TW-NOTA 247, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

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
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2006-01-13
FZY	Hammer, Surgical	General, Plastic Surgery	Class 1	878.4800	1994-08-08
GWX	Fork, Tuning	Neurology	Class 1	882.1525	2006-01-13
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	1994-08-08
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2011-11-07
FMA	Depressor, Tongue, Non-Surgical	General Hospital	Class 1	880.6230	2006-01-13
LRW	Scissors, General, Surgical	General, Plastic Surgery	Class 1	878.4800	2013-01-02

Official Correspondent

No official correspondent registered.

US Agent Details

Jennifer Reich Business: Harvest & Victory Consulting Corp.(USA) Email: ftcr67@gmail.com Phone: (928) 8638140

Related Public Records

Same Entity

CHIN KOU MEDICAL INSTRUMENT CO.,LTD.

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
K932506	Rudolf Riester GmbH & Co. KG	RI-SCOPE (S)	1993-10-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003782614. Last updated year: 2026. Please use registration number 3003782614 when referencing this establishment in official correspondence.