Data / Medical devices / Latex Patient Examination Glove / China
FDA-registered makers of Latex Patient Examination Glove in China: 9 establishments
9 establishments in China are registered with the FDA to make Latex Patient Examination Glove (product code LYY). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Latex Patient Examination Glove
- Product code
- LYY
- Country
- China
Makers of Latex Patient Examination Glove in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Shandong Intco Medical Products Co Ltd | Qingzhou Shandong, China | Manufacturer | 2 | February 22, 2023 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Jinxiang Latex Products Co., Ltd. | Shanghai, China | Contract manufacturer, Exporter to the US, Manufacturer | 2 | October 31, 1989 | 0 | 0 | 0 | api.fda.gov |
| Motex Healthcare (anhui) Co., Ltd. | Guangde City, Xuancheng City Anhui, China | Exporter to the US, Manufacturer | 1 | December 2, 2002 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Motex Healthcare Co., Ltd. | Shanghai, China | Exporter to the US, Manufacturer | 1 | December 2, 2002 | 0 | 0 | 0 | api.fda.gov |
| Alcatron Gloves Factory | Weifang Shandong, China | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangzhou Noval Medical Co., Ltd. | GUANGZHOU Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Huizhou Anboson Technology Co., Ltd. | huizhou Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhangjiagang Dayu Rubber Products Co., Ltd. | ZHANGJIAGANG CITY Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zibo Blue Sail Health Technology Co., Ltd | Zibo Shandong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.