Data / Medical devices / China / Wuhan Hongjian Co., Ltd.
Wuhan Hongjian Co., Ltd.: FDA-registered device maker in Wuhan Hubei, China, 1 510(k) clearance
Wuhan Hongjian Co., Ltd. is registered with the FDA (registration 3037028694) in Wuhan Hubei, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 25, 2023. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3037028694
- Address
- Building B1, Guanlianhu Road, Economic & Technological Development, Wuhan, Hubei, Wuhan Hubei, China, 430056
- Owner or operator
- Wuhan Hongjian Co., Ltd. (10092838)
- Roles
- Manufacturer
- First device listed
- May 29, 2025
- Registered through
- 2027
- Brand names listed
- Vinyl Exam Gloves
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vinyl Patient Examination Glove | LYZ | 1 | Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 25, 2023 | K230046 | Vinyl examination gloves | LYZ | Substantially Equivalent | Guangdong Kingfa Sci. & Tech.Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated March 25, 2023. 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.