KANGFU MEDICAL EQUIPMENT FACTORY

FDA Device Registration & Listing · Wenzhou Zhejiang, CN · Registration 3015140207

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015140207
FEI Number
3015140207
Entity Name
KANGFU MEDICAL EQUIPMENT FACTORY
City/State/Country
Wenzhou Zhejiang, CN
Establishment Address
No.380 Ningkang East Road, Yueqing, Wenzhou Zhejiang 325600, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Kangfu Medical Equipment Factory (Owner Number: 10059139)
Owner / Operator Contact Address
No.380 Ningkang East Road, Yueqing, Wenzhou, CN-ZJ 325600, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

KFT-16 KFT-17 KFT-18 KFT-22 KFT-22M KFT-23 KFT- 24 KFT-25 KFT-26 KFT-27 KFT-28 KFT-01 KFT-02 KFT-03 KFT-03C KFT-04 KFT-05 KFT-05L KFT-06 KFT-07 KFT-08 KFT-09 KFT-10 KFT-11 KFT-12 KFT-13 KFT-14 KFT-15 Hearing Aid, Air-Conduction, Prescription Hearing Aid, Air-Conduction with Wireless Technology, Prescription Hearing Aid, Air-Conduction, Over the Counter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SDV Clinical Electronic Thermometer General Hospital Class 2 880.2910 2025-07-04
ESD Hearing Aid, Air-Conduction, Prescription Ear, Nose, Throat Class 1 874.3300 2025-01-09
FLL Continuous Measurement Thermometer General Hospital Class 2 880.2910 2022-03-16
OSM Hearing Aid, Air-Conduction With Wireless Technology, Prescription Ear, Nose, Throat Class 2 874.3305 2025-01-09
QUF Hearing Aid, Air-Conduction, Over The Counter Ear, Nose, Throat Class 1 874.3300 2025-01-09

Official Correspondent

Anthony Pan

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: Regrek.Cs@Hotmail.Com Phone: (302) 6089028

Related Public Records

Same Entity

Kangfu Medical Equipment Factory
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
K892457 Telstar Electronics, Inc. TELSTAR MODEL 1/3 ITE HEARING AID 1989-06-06
K760996 Unitron Industries, Inc. HEARING AID (MODEL 695D, 905 & 960P) 1976-11-16
K840825 Maico Hearing Instruments, Inc. SERIES MR IN-THE-EAR CUSTOM HEARING AID 1984-03-30
K946253 Maico Hearing Instruments, Inc. MAICO IN-THE-EAR MODEL RD 201 1995-01-30
K863975 Gn Danavox, Inc. CUSTOM IN-THE-EAR 1986-11-07

Similar Registrations

Registration Number Establishment Name Location
3030989301 TRIMEDIKA LTD Belfast Mid Ulster, GB
3021042343 HUAIAN ZHONGXIN PACKING MATERIAL CO., LTD. Huaian Jiangsu, CN
3010852191 HONG KONG MEDSOURCING LIMITED KOWLOON, HK
3007499349 VERIDIAN HEALTHCARE Gurnee, IL, US
3008573045 Andon Medical co., LTD Tianjin, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015140207. Last updated year: 2026. Please use registration number 3015140207 when referencing this establishment in official correspondence.
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