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Data / Medical devices / China / Suzhou ZhongJing Life & Science Technology Co., Ltd.

Suzhou ZhongJing Life & Science Technology Co., Ltd.: FDA-registered device maker in Suzhou City Jiangsu, China, 1 510(k) clearance

Suzhou ZhongJing Life & Science Technology Co., Ltd. is registered with the FDA (registration 3004116023) in Suzhou City Jiangsu, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 18, 2002. Registered through 2027. FDA data exported November 3, 2026.

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FDA registration number
3004116023
Address
197 Lianhua Road, Songling Town Wujiang District, Suzhou City Jiangsu, China, 215222
Owner or operator
Suzhou Zhongjing Life & Science Technology Co., Ltd. (9048583)
Roles
Exporter to the US, Manufacturer
First device listed
November 3, 2007
Registered through
2027
Brand names listed
Aculine, Aculux, Altra, QIZHOU AND UNICO ACUPUNCTURE NEEDLE

Devices it lists

DeviceProduct codeClassRoleSource
Needle, Acupuncture, Single UseMQX2Exporter to the US, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
July 18, 2002K013926QIZHOU ACUPUNCTURE NEEDLEMQXSubstantially EquivalentWujiang City Shenli Medical and Health Material COaccessdata.fda.gov

Compare with other makers

Updated July 18, 2002. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.