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Data / Medical devices / China / Jiangsu Ideal Medical Science & Technology Co., Ltd.

Jiangsu Ideal Medical Science & Technology Co., Ltd.: FDA-registered device maker in Zhangjiagang City Jiangsu, China, 3 510(k) clearances

Jiangsu Ideal Medical Science & Technology Co., Ltd. is registered with the FDA (registration 3010606097) in Zhangjiagang City Jiangsu, China. It lists 7 device types. The FDA files 3 510(k) clearances under its listings, the newest dated March 3, 2015. Registered through 2026. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3010606097
Address
East Area, Jinfeng Industry Park, Zhangjiagang City Jiangsu, China, 215625
Owner or operator
Jiangsu Ideal Medical Science & Technology Co., Ltd. (10051336)
Roles
Contract manufacturer, Manufacturer
First device listed
March 3, 2016
Registered through
2026
Brand names listed
AxCess® Expandable Interbody System, Bone Curette, Ideal

Devices it lists

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
March 3, 2015K141825IDEAL Locking Plate SystemHRSSubstantially EquivalentJiangsu Ideal Medical Science & Technology Co., LTaccessdata.fda.gov
January 30, 2015K142957Ideal pedicle screw spinal systemMNHSubstantially EquivalentJiangsu Ideal Medical Science & Technology Co., Ltd.accessdata.fda.gov
December 20, 2013K132428IDEALHSBSubstantially EquivalentJiangsu Ideal Medical Science & Technology Co., LTaccessdata.fda.gov

Compare with other makers

Updated March 3, 2015. 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.