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Data / Medical devices / China / Jiujiang Huada Medical Dressing Co., Ltd.

Jiujiang Huada Medical Dressing Co., Ltd.: FDA-registered device maker in JIUJIANG Jiangxi, China, 2 510(k) clearances

Jiujiang Huada Medical Dressing Co., Ltd. is registered with the FDA (registration 3004753358) in JIUJIANG Jiangxi, China. It lists 18 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 25, 2018. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

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FDA registration number
3004753358
Address
Minjiashan Road, Gongqingcheng, JIUJIANG Jiangxi, China, 332020
Owner or operator
JUJIANG HUADA MEDICAL DRESSING CO., LTD. (9066457)
Roles
Contract manufacturer, Manufacturer
First device listed
September 8, 2004
Registered through
2026
Brand names listed
Barrier Film, Bed Cover, Bed Sheet, Bib Clip, COTTON BALL, COTTON ROLL, COTTON WOOL, CSR wrap and more

Devices it lists

DeviceProduct codeClassRoleSource
Absorber, Saliva, PaperKHR1Contract manufacturer, Manufactureraccessdata.fda.gov
Accessory, Surgical ApparelLYU1Contract manufacturer, Manufactureraccessdata.fda.gov
Applicator, Absorbent Tipped, Non-SterileKXF1Contract manufacturer, Manufactureraccessdata.fda.gov
Bandage, CastITG1Manufactureraccessdata.fda.gov
Bandage, ElasticFQM1Contract manufacturer, Manufactureraccessdata.fda.gov
Bedding, Disposable, MedicalKME1Contract manufacturer, Manufactureraccessdata.fda.gov
Cap, SurgicalFYF1Contract manufacturer, Manufactureraccessdata.fda.gov
Component, CastLGF1Contract manufacturer, Manufactureraccessdata.fda.gov
Cotton, RollEFN1Contract manufacturer, Manufactureraccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Contract manufacturer, Manufactureraccessdata.fda.gov
Gauze/Sponge, Internal, X-Ray DetectableGDY1Manufactureraccessdata.fda.gov
Mask, SurgicalFXX2Manufactureraccessdata.fda.gov
Mouthpiece, Saliva EjectorDYN1Contract manufacturer, Manufactureraccessdata.fda.gov
Non-Surgical GownOEA1Manufactureraccessdata.fda.gov
Respirator, SurgicalMSH2Manufactureraccessdata.fda.gov
Shoe And Shoe Cover, ConductiveBWP1Manufactureraccessdata.fda.gov
Unit, Operative Dental, AccessoriesNRD1Contract manufacturer, Manufactureraccessdata.fda.gov
Wrap, SterilizationFRG2Manufactureraccessdata.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
January 25, 2018K173062Non Woven Face Mask (Models: VQN0185W (earloop) and VQN0185B (ties))FXXSubstantially EquivalentV&Q Manufacturing Corporationaccessdata.fda.gov
December 27, 2007K071886SELF SEAL STERILIZATION POUCHFRGSubstantially EquivalentShanghai Jianzhong Medical Packaging Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated January 25, 2018. 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.