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Touchstone International Medical Science Co., Ltd.: FDA-registered device maker in Suzhou Jiangsu, China, 2 510(k) clearances

Touchstone International Medical Science Co., Ltd. is registered with the FDA (registration 3007222388) in Suzhou Jiangsu, China. It lists 6 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 26, 2014. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3007222388
Address
278 Dongping Street, Suzhou Industrial Park, Suzhou Jiangsu, China, 215123
Owner or operator
Touchstone International Medical Science Co., Ltd. (10027069)
Roles
Manufacturer
First device listed
September 24, 2008
Registered through
2027
Brand names listed
Auto Purse String Clamp for Single Use, CLC Series Curved Linear Cutter and Reloads, CSC Series Intraluminal Stapler for Single Use, CST Series Intraluminal Stapler for Single Use, Circumcision Stapler for Single Use, ELC, FELC and SELC Series Endoscopic Linear Cutter and Single Use Loading Unit, LC Series Linear Cutter and Reloads, LS Series Linear Stapler and Reloads and more

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
September 26, 2014K141097CSC SERIES INTRALUMINAL STAPLER FOR SINGLE USEGDWSubstantially EquivalentTouchstone International Medical Science Co., Ltd.accessdata.fda.gov
July 25, 2014K141367LS SERIES LINEAR STAPLER AND RELOADS, CLC SERIES CURVED LINEAR CUTTER AND RELOADS, LC SERIES LINEAR CUTTER AND RELOADSGDWSubstantially EquivalentTouchstone International Medical Science Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 26, 2014. 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.