YONGKANG JINKANG HEALTH EQUIPMENT FACTORY

FDA Device Registration & Listing · Yongkang Zhejiang, CN · Registration 3009109626

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
3009109626
FEI Number
3009109626
Entity Name
YONGKANG JINKANG HEALTH EQUIPMENT FACTORY
City/State/Country
Yongkang Zhejiang, CN
Establishment Address
No.18 Jiulong Hu North Road,East District, Yongkang Zhejiang 321300, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Yongkang Jinkang Health Equipment Factory (Owner Number: 10036460)
Owner / Operator Contact Address
No.18 Jiulong Hu North Road,East District, Yongkang, CN-ZJ 321300, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

JK6, JK12, JK18, JK24, JK32, ABC001, ABC002, ABC003, ABC004, ABC005, ABC006, ABC007, ABC008, ABC009, AW-6, AW-12, AW-18 1pcs,2pcs,4pcs,6pcs,8pcs,10pcs,12pcs,16pcs,18pcs,20pcs,24pcs,26pcs,28pcs,30pcs,32pcs,48pcs Scraping board Blood collection pen Nasal irrigator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNM Device, Pressure Applying Physical Medicine Class 1 890.5765 2011-05-09
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature General, Plastic Surgery Class 2 878.4850 2019-11-14
KAR Irrigator, Sinus Ear, Nose, Throat Class 1 874.4420 2019-05-20

Official Correspondent

No official correspondent registered.

US Agent Details

Kai Li Email: likai323@hotmail.com Phone: (501) 7778490

Related Public Records

Same Entity

Yongkang Jinkang Health 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
K130132 Medipurpose Pte. , Ltd. BABYLANCE HEEL INCISION DEVICE 2013-02-11

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0044-2008 Becton Dickinson & Company 2
Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

Similar Registrations

Registration Number Establishment Name Location
9612390 Wujiang City Shen Ling Medical Device Co.,Ltd. Suzhou Jiangsu, CN
3015422337 XIAMEN FIRSTCARE IMP. & EXP. CO.,LTD. Xiamen Fujian, CN
3010673773 Ningbo Troika Science & Technology Co.,Ltd. Ningbo Zhejiang, CN
3013397886 ADVANCE-ESTHETIC LLC Fort Lauderdale, FL, US
3033450607 DONGGUAN XILIJIAN TECHNOLOGY CO., LTD. Dongguan Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009109626. Last updated year: 2026. Please use registration number 3009109626 when referencing this establishment in official correspondence.
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