Data / Medical devices / Pad, Menstrual, Scented, Scented-Deodorized / China
FDA-registered makers of Pad, Menstrual, Scented, Scented-Deodorized in China: 8 establishments
8 establishments in China are registered with the FDA to make Pad, Menstrual, Scented, Scented-Deodorized (product code HHL). 0 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
- Pad, Menstrual, Scented, Scented-Deodorized
- Product code
- HHL
- Country
- China
Makers of Pad, Menstrual, Scented, Scented-Deodorized in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Fujian Hui'an Hecheng Household Products Co., Ltd | Quanzhou Fujian, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong Bainuo Sanitary Product Co., Ltd. | Foshan Guangdong, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong Kawada Sanitary Products Co.,Ltd. Southern District Branch Company. | GUANG DONG Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hebei Yihoucheng Commodity Co., Ltd. | Baoding Hebei, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kunshan Yari Sanitary Products Co., Ltd. | Kunshan Jiangsu, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| RFI Hygiene Limited | Shanghai, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Shuxiao Industry Co.,ltd | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhejiang Shuxiao Personal Hygiene Products Co., Ltd | Jiashan Zhejiang, 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.