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
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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 22, 2026 | K253773 | Guanhong 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); Guanhong | MMK | Substantially Equivalent | Taizhou Huangyan Guanhong Plastic Steel Products Factory | accessdata.fda.gov |
Compare with other makers
- All makers of Crutch
- All makers of System, Blood Collection, Vacuum-Assisted, Manual
- All makers of Container, Sharps
- All makers of Forceps
- All makers of Basin, Emesis
- All makers of Tray, Surgical, Instrument
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.