Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014632466

FEI Number

3014632466

Entity Name

GUANGDONG KEGAO ELECTRONICS CO.,LTD.

City/State/Country

Foshan Guangdong, CN

Establishment Address

No.39 East Sci-Tech Avenue, Zone A, Shishan Sci-Tech Industrial Park, Shishan Town, Nanhai District, Foshan Guangdong 528225, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

GUANGDONG KEGAO ELECTRONICS CO.,LTD. (Owner Number: 10092448)

Owner / Operator Contact Address

No.39 East Sci-Tech Avenue, Zone A, Shishan Sci-Tech Industrial Park, Shishan Town, Nanhai District,, Foshan, CN-GD 528225, 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	2025-01-09

Official Correspondent

Becky Yuan

US Agent Details

Dale Li Business: HTT TECHNOLOGIES INC. Email: emily.zhang@3hmedical.com Phone: (984) 6662381

Related Public Records

Same Entity

GUANGDONG KEGAO ELECTRONICS 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 3014632466. Last updated year: 2026. Please use registration number 3014632466 when referencing this establishment in official correspondence.