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Data / Medical devices / China / Yinghua Medical Products Co., Ltd.

Yinghua Medical Products Co., Ltd.: FDA-registered device maker in huaibei Anhui, China, 4 510(k) clearances

Yinghua Medical Products Co., Ltd. is registered with the FDA (registration 3030214028) in huaibei Anhui, China. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 27, 2017. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3030214028
Address
NO 22 Longwang Road,Longhu Industrial Park,Huaibei City,Anhui, huaibei Anhui, China, 235000
Owner or operator
YINGHUA MEDICAL MEDICAL PRODUCTS CO., LTD. (10089146)
Roles
Manufacturer
First device listed
November 9, 2023
Registered through
2026
Brand names listed
Patient Nitrile Examination Gloves, Powder Free, Non-Sterile Blue Color, Patient Vinyl Examination Gloves, Powder Free, Non-Sterile

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
June 27, 2017K170735Powder-Free Clear Vinyl Patient Examination GlovesLYZSubstantially EquivalentZibo Yue Fan Medical Products Co, Ltd.accessdata.fda.gov
February 5, 2016K153028Synmax Synthetic Patient Examination Vinyl Gloves, Powder Free, BlueLYZSubstantially EquivalentZibo Huiying Medical Products, Co. , Ltd.accessdata.fda.gov
May 6, 2014K122656POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, YELLOW COLORLYZSubstantially EquivalentShandong Yifan Plastic Products Co., Ltd.accessdata.fda.gov
February 28, 2013K123869POWDER-FREE NITRILE PATIENT EXAMINATION GLOVESLZASubstantially EquivalentDehai (Shandong) Medical Gloves, Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated June 27, 2017. 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.