Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002798681

FEI Number

3002798681

Entity Name

KUO TONG ELECTRICALTECHNOLOGY (HUI ZHOU) CO., LTD.

City/State/Country

HUIZHOU CITY Guangdong, CN

Establishment Address

No.442,Yongping Road, Xiufeng Village, Liangjing Town, HUIZHOU CITY Guangdong 516265, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Kuo Tong Electrical Technology (HuiZhou) Co., Ltd. (Owner Number: 9052879)

Owner / Operator Contact Address

3F Guangcheng Commercial Bldg, Jinhui Rd, Danshui Town, Huiyang, Huizhou City, CN-GD 516211, CN

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
KFZ	Humidifier, Non-Direct Patient Interface (Home-Use)	Anesthesiology	Class 1	868.5460	2002-09-07

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Kuo Tong Electrical Technology (HuiZhou) Co., Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002798681. Last updated year: 2026. Please use registration number 3002798681 when referencing this establishment in official correspondence.