Data / Medical devices / Tampon, Menstrual, Unscented / China
FDA-registered makers of Tampon, Menstrual, Unscented in China: 8 establishments
8 establishments in China are registered with the FDA to make Tampon, Menstrual, Unscented (product code HEB). 8 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
- Tampon, Menstrual, Unscented
- Product code
- HEB
- Country
- China
Makers of Tampon, Menstrual, Unscented in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Guangdong Bingbing Health Care Products Ltd. | Jiangmen Guangdong, China | Exporter to the US, Manufacturer, Repackager or relabeler | 6 | December 15, 2023 | 0 | 0 | 0 | api.fda.gov |
| Suzhou Borage Medical Technology Co.,ltd. | Suzhou Jiangsu, China | Exporter to the US, Manufacturer | 4 | May 10, 2024 | 0 | 0 | 0 | api.fda.gov |
| Unibeauty (hubei) Technology Co., Ltd. | Xiantao Hubei, China | Exporter to the US, Manufacturer | 4 | December 17, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shandong Intco Hygiene Products Co., Ltd. | Zibo Shandong, China | Contract manufacturer, Manufacturer | 2 | January 10, 2025 | 0 | 0 | 0 | api.fda.gov |
| Fujian Time And Tianhe Industrial Co., Ltd | Nanan Fujian, China | Exporter to the US, Manufacturer, Repackager or relabeler | 1 | September 30, 2022 | 0 | 0 | 0 | api.fda.gov |
| Fujian Tonggang Industries Ltd. | Quanzhou Fujian, China | Exporter to the US, Manufacturer | 1 | August 13, 2025 | 0 | 0 | 0 | api.fda.gov |
| Hangzhou Pengtu Chemical Fiber Co.,ltd | Hangzhou Zhejiang, China | Manufacturer | 1 | August 14, 2023 | 0 | 0 | 0 | api.fda.gov |
| Zhejiang Tianqing Manufacturing Technology Group Co.,ltd. | Huzhou Zhejiang, China | Specification developer | 1 | August 14, 2023 | 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.