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Data / Medical devices / China / Motex Healthcare (anhui) Co., Ltd.

Motex Healthcare (anhui) Co., Ltd.: FDA-registered device maker in Guangde City, Xuancheng City Anhui, China, 9 510(k) clearances

Motex Healthcare (anhui) Co., Ltd. is registered with the FDA (registration 3014269027) in Guangde City, Xuancheng City Anhui, China. It lists 4 device types. The FDA files 9 510(k) clearances under its listings, the newest dated May 23, 2022. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3014269027
Address
Xinhang Economic Development Zone, Guangde City, Xuancheng City Anhui, China, 242234
Owner or operator
Motex Healthcare (Anhui) Co., Ltd. (10056753)
Roles
Exporter to the US, Manufacturer
First device listed
January 11, 2018
Registered through
2026
Brand names listed
Latex Patient Examination Glove, Polymer Patient Examination Glove, Powder-free Nitrile Examination Gloves Tested for use with Chemotherapy Drugs, Surgeon's Glove

Devices it lists

DeviceProduct codeClassRoleSource
Latex Patient Examination GloveLYY1Exporter to the US, Manufactureraccessdata.fda.gov
Medical Glove, SpecialtyLZC1Exporter to the US, Manufactureraccessdata.fda.gov
Polymer Patient Examination GloveLZA1Exporter to the US, Manufactureraccessdata.fda.gov
Surgeon'S GlovesKGO1Exporter to the US, Manufactureraccessdata.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
May 23, 2022K220155Powder-free Nitrile Examination Gloves Tested for use with Chemotherapy DrugsLZASubstantially EquivalentMotex Healthcare (Anhui) Co., Ltd.accessdata.fda.gov
June 4, 2014K123126MOTEX POLYISOPRENE POWDER-FREE SURGICAL GLOVES MODEL # 6412(6432) AND # 6512(6532)KGOSubstantially EquivalentShanghai Motex Healthcare Co., Ltd.accessdata.fda.gov
May 21, 2014K132802MOTEX POWDERED NITRILE SURGICAL GLOVESKGOSubstantially EquivalentShanghai Motex Healthcare Co., Ltd.accessdata.fda.gov
October 3, 2013K122557MOTEX POWDER-FREE NITRILE SURGICAL GLOVESKGOSubstantially EquivalentShanghai Motex Healthcare Co., Ltd.accessdata.fda.gov
July 27, 2007K063757MOTEX POWDER-FREE SURGICAL GLOVES AND LIGHTLY POWDERED SURGICAL GLOVESKGOSubstantially EquivalentShanghai Motex Healthcare Co., Ltd.accessdata.fda.gov
August 20, 2004K041276POWDER-FREE NITRILE EXAMINATION GLOVESLZASubstantially EquivalentShanghai Motex Healthcare Co., Ltd.accessdata.fda.gov
May 2, 2003K030207NITRILE POWDER-FREE EXAMINATION GLOVES, PROBLUE, #7235 7 #7735LZASubstantially EquivalentShanghai Motex Healthcare Co., Ltd.accessdata.fda.gov
December 2, 2002K020837MOTEX LATEX EXAMINATION GLOVES, POWDER-FREELYYSubstantially EquivalentShanghai Motex Healthcare Co., Ltd.accessdata.fda.gov
November 29, 2001K013261MOTEX NITRILE EXAMINATION GLOVES POWDER-FREELZASubstantially EquivalentShanghai Motex Healthcare Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 23, 2022. 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.