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Data / Medical devices / China / Hebei Changsheng Plastic Products Co.,Ltd.

Hebei Changsheng Plastic Products Co.,Ltd.: FDA-registered device maker in xingtai Hebei, China, 1 510(k) clearance

Hebei Changsheng Plastic Products Co.,Ltd. is registered with the FDA (registration 3009709178) in xingtai Hebei, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 27, 2012. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3009709178
Address
No 99, Huangjin Avenue, Julu County, xingtai Hebei, China, 055250
Owner or operator
Hebei Changsheng Plastic Products Co.,Ltd. (10041213)
Roles
Manufacturer
First device listed
July 2, 2012
Registered through
2026
Brand names listed
Vinyl patient examination glove

Devices it lists

DeviceProduct codeClassRoleSource
Vinyl Patient Examination GloveLYZ1Manufactureraccessdata.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
April 27, 2012K113837POWDER FREE VINYL PATIENT EXAMINATION GLOVESLYZSubstantially EquivalentHebei Changsheng Plastic Products Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 27, 2012. 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.