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Data / Medical devices / China / Taizhou Huangyan Guanhong Plastic Steel Products Factory

Taizhou Huangyan Guanhong Plastic Steel Products Factory: FDA-registered device maker in Taizhou Zhejiang, China, 1 510(k) clearance

Taizhou Huangyan Guanhong Plastic Steel Products Factory is registered with the FDA (registration 3030519472) in Taizhou Zhejiang, China. It lists 16 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 22, 2026. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3030519472
Address
Chengjiang Street Industrial Park, Huangyan District, Taizhou Zhejiang, China, 318020
Owner or operator
Taizhou Huangyan Guanhong Plastic Steel Products Factory (10089732)
Roles
Contract manufacturer, Manufacturer
First device listed
January 3, 2024
Registered through
2026
Brand names listed
24 hour Urine Collection Bottles, Bed Pad, Centrifuge tube, Collection Funnel with Filter, Emesis Basin Mauve, Graduated Triangular Intake, Guanhong Sharps Container, Guidewire Bowls and more

Devices it lists

DeviceProduct codeClassRoleSource
Basin, EmesisFNY1Contract manufacturer, Manufactureraccessdata.fda.gov
Bedding, Disposable, MedicalKME1Contract manufacturer, Manufactureraccessdata.fda.gov
BedpanFOB1Contract manufacturer, Manufactureraccessdata.fda.gov
Catheter, IrrigationGBX1Contract manufacturer, Manufactureraccessdata.fda.gov
Container, Liquid Medication, GraduatedKYW1Contract manufacturer, Manufactureraccessdata.fda.gov
Container, SharpsMMK2Manufactureraccessdata.fda.gov
Container, Specimen, Non-SterileNNI1Contract manufacturer, Manufactureraccessdata.fda.gov
Container, Specimen, SterileFMH1Contract manufacturer, Manufactureraccessdata.fda.gov
CrutchIPR1Contract manufacturer, Manufactureraccessdata.fda.gov
Dispenser, Liquid MedicationKYX1Contract manufacturer, Manufactureraccessdata.fda.gov
ForcepsHTD1Contract manufacturer, Manufactureraccessdata.fda.gov
Light, Surgical HeadlightEBA1Contract manufacturer, Manufactureraccessdata.fda.gov
Mattress, Flotation Therapy, Non-PoweredIKY1Contract manufacturer, Manufactureraccessdata.fda.gov
Pipette, PasteurGJW1Contract manufacturer, Manufactureraccessdata.fda.gov
System, Blood Collection, Vacuum-Assisted, ManualKST1Contract manufacturer, Manufactureraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Contract manufacturer, 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 22, 2026K253773Guanhong Sharps Container (GHW-1F1); Guanhong Sharps Container (GHW-1F4); Guanhong Sharps Container (GH-6FA); Guanhong Sharps Container (GHW-2FR); Guanhong Sharps Container (GHW-8FR); Guanhong Sharps Container (GH-3FS); Guanhong Sharps Container (GHW-15FS); Guanhong Sharps Container (GHW-27FS); Guanhong Sharps Container (GH-5FSW); Guanhong Sharps Container (GHW-3FT); Guanhong Sharps Container (GHW-4FT); Guanhong Sharps Container (GHW-5FT); Guanhong Sharps Container (GHW-8FT); GuanhongMMKSubstantially EquivalentTaizhou Huangyan Guanhong Plastic Steel Products Factoryaccessdata.fda.gov

Compare with other makers

Updated May 22, 2026. 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.