Data / Medical devices / China / Anhui Hongyuan Medical Products Co., Ltd.
Anhui Hongyuan Medical Products Co., Ltd.: FDA-registered device maker in Huaibei Anhui, China, 3 510(k) clearances
Anhui Hongyuan Medical Products Co., Ltd. is registered with the FDA (registration 3029952429) in Huaibei Anhui, China. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated January 7, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3029952429
- Address
- No.121 Suixi Middle Road, Suixi County, Huaibei City, Anhui Province, Huaibei Anhui, China, 235100
- Owner or operator
- ANHUI HONGYUAN MEDICAL MEDICAL PRODUCTS CO., LTD. (10088761)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- October 9, 2023
- Registered through
- 2026
- Brand names listed
- Patient Vinyl Examination Gloves, Powder Free, Non-Sterile, Vinyl patient examination glove
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Vinyl Patient Examination Glove | LYZ | 1 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| January 7, 2014 | K131832 | POWDER-FREE VINYL PATIENT EXAMINATION GLOVES | LYZ | Substantially Equivalent | Shandong Binxiang Medical Products Co., Ltd. | accessdata.fda.gov |
| June 17, 2013 | K123590 | VINYL EXAMINATION POWDER FREE GLOVES, CLEAR | LYZ | Substantially Equivalent | Weilin Plastic and Rubber Products Co., Ltd. | accessdata.fda.gov |
| July 15, 2011 | K110857 | POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, YELLOW COLOR | LYZ | Substantially Equivalent | Shandong Zhanpeng Medical Products Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated January 7, 2014. 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.