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Data / Medical devices / China / Inpro Technology Device Factory

Inpro Technology Device Factory: FDA-registered device maker in WEIFANG Shandong, China, 2 510(k) clearances

Inpro Technology Device Factory is registered with the FDA (registration 3009512322) in WEIFANG Shandong, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 23, 2016. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3009512322
Address
No.10-1, Xingan Road East, Linqu, WEIFANG Shandong, China, 262600
Owner or operator
INPRO TECHNOLOGY DEVICE FACTORY (10039198)
Roles
Manufacturer
First device listed
December 16, 2011
Registered through
2026
Brand names listed
Inpro, omnishield

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
June 23, 2016K160468Synthetic Vinyl Examination Gloves, Powder-Free, YellowLYZSubstantially EquivalentInpro Technology Device Factoryaccessdata.fda.gov
December 5, 2011K112610SYNTHETIC VINYL EXAMINATION GLOVES, POWDER FREE (AND MULTIPLE LABELS)LYZSubstantially EquivalentInpro Technology Device Factoryaccessdata.fda.gov

Compare with other makers

Updated June 23, 2016. 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.