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Data / Medical devices / China / Liao Ning Shangwei Medical Products Co., Ltd

Liao Ning Shangwei Medical Products Co., Ltd: FDA-registered device maker in Tieling Liaoning, China, 1 510(k) clearance

Liao Ning Shangwei Medical Products Co., Ltd is registered with the FDA (registration 3020677870) in Tieling Liaoning, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 20, 2021. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3020677870
Address
North West of Xinlixian,Quanyangou Village Xiaonan Town,Diaobingshan City, Tieling Liaoning, China, 112700
Owner or operator
Liao Ning Shangwei Medical Products Co., Ltd (10084919)
Roles
Manufacturer
First device listed
April 15, 2022
Registered through
2026
Brand names listed
Powder Free Vinyl Patient Examination Gloves, Clear (non-colored)

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
December 20, 2021K211865Powder Free Vinyl Patient Examination Gloves, Clear (non-colored)LYZSubstantially EquivalentLiao Ning Shangwei Medical Products Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 20, 2021. 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.