Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004116023

FEI Number

3004116023

Entity Name

Suzhou ZhongJing Life & Science Technology Co., Ltd.

City/State/Country

Suzhou City Jiangsu, CN

Establishment Address

197 Lianhua Road, Songling Town, Wujiang District, Suzhou City Jiangsu 215222, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Suzhou Zhongjing Life & Science Technology Co., Ltd. (Owner Number: 9048583)

Owner / Operator Contact Address

197 Lianhua Road,, Songling Town Wujiang District, Suzhou City Jiangsu, CN-NOTA 215222, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K013926

PMA Number

N/A

All Registered Proprietary Names

QIZHOU AND UNICO ACUPUNCTURE NEEDLE Altra Aculine Aculux

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQX	Needle, Acupuncture, Single Use	General Hospital	Class 2	880.5580	2007-11-03

Official Correspondent

No official correspondent registered.

US Agent Details

Jim MacNee Business: USDeviceAgent.com Email: Jmacnee@USDeviceAgent.com Phone: (951) 8486626

Related Public Records

Same Entity

Suzhou Zhongjing Life & Science Technology 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 3004116023. Last updated year: 2026. Please use registration number 3004116023 when referencing this establishment in official correspondence.