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Data / Medical devices / China / Ever Light Plastic Products Co., Ltd.

Ever Light Plastic Products Co., Ltd.: FDA-registered device maker in Shijiazhuang Hebei, China, 8 510(k) clearances

Ever Light Plastic Products Co., Ltd. is registered with the FDA (registration 3005596481) in Shijiazhuang Hebei, China. It lists 2 device types. The FDA files 8 510(k) clearances under its listings, the newest dated December 18, 2014. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3005596481
Address
Donggao Industrial Zone, zanhuang, Shijiazhuang Hebei, China, 050000
Owner or operator
EVER LIGHT PLASTIC PRODUCTS CO., LTD. (9083042)
Roles
Contract manufacturer, Manufacturer
First device listed
December 28, 2007
Registered through
2026

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
December 18, 2014K142570Powder Free Vinyl Patient Examination Gloves ( Yellow, White, BLue, Pink )LYZSubstantially EquivalentEver Light Plastic Products Co., Ltd.accessdata.fda.gov
December 17, 2014K142571Powder Free Vinyl Patient Examination GlovesLYZSubstantially EquivalentEver Light Plastic Products Co., Ltd.accessdata.fda.gov
October 29, 2010K102655POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH ALOE VERA (YELLOW, WHITE, BLUE)LYZSubstantially EquivalentEver Light Plastic Products Co., Ltd.accessdata.fda.gov
September 26, 2008K082029SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVELYZSubstantially EquivalentEver Light Plastic Products Co., Ltd.accessdata.fda.gov
December 5, 2006K063213EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDER FREE (WHITE) VINYL PATIENT EXAMINATION GLOVESLYZSubstantially EquivalentEver Light Plastic Products Co., Ltd.accessdata.fda.gov
July 7, 2006K060785POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES W/ALOE VERA, GREEN COLORLYZSubstantially EquivalentEver Light Plastic Products Co., Ltd.accessdata.fda.gov
May 8, 2006K060786SYNTHETIC (YELLOW) VINYL PATIENT EXAMINATION GLOVE-POWDER FREELYZSubstantially EquivalentEver Light Plastic Products Co., Ltd.accessdata.fda.gov
April 28, 2006K060778SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWDER FREELYZSubstantially EquivalentEver Light Plastic Products Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 18, 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.