Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013002100

FEI Number

3013002100

Entity Name

JIANGXI YIKANG MEDICAL INSTRUMENT GROUP CO., LTD.

City/State/Country

Nanchang Jiangxi, CN

Establishment Address

No.188 LiduAihua Ave., Jinxian County, Nanchang Jiangxi 331725, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Jiangxi Yikang Medical Instrument Group Co., LTD. (Owner Number: 10051716)

Owner / Operator Contact Address

No.188 LiduAihua Ave., Jinxian County, Nanchang, CN-JX 331725, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K173340

PMA Number

N/A

All Registered Proprietary Names

Latex Foley Catheter

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EZL	Catheter, Retention Type, Balloon	Gastroenterology, Urology	Class 2	876.5130	2018-07-13

Official Correspondent

Dashan Qiang

US Agent Details

Phoenix Wang Email: wcy_2@hotmail.com Phone: (405) 6945955

Related Public Records

Same Entity

Jiangxi Yikang Medical Instrument Group 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
K233013	Silq Technologies Corporation	2-Way 100% Silicone Cleartract Catheter	2024-01-23

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1018233	C.R. BARD, INC.	COVINGTON, GA, US
3010400865	WELL LEAD MEDICAL CO. LTD	GUANGZHOU Guangdong, CN
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013002100. Last updated year: 2026. Please use registration number 3013002100 when referencing this establishment in official correspondence.