Data / Medical devices / Lubricant, Personal / China
FDA-registered makers of Lubricant, Personal in China: 10 establishments
10 establishments in China are registered with the FDA to make Lubricant, Personal (product code NUC). 7 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
- Lubricant, Personal
- Product code
- NUC
- Country
- China
Makers of Lubricant, Personal in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Foshan Pingchuang Medical Technology Co., Ltd | Foshan City Guangdong, China | Manufacturer | 2 | December 15, 2025 | 0 | 0 | 0 | api.fda.gov |
| BATH CONCEPTS COSMETICS (DongGuan) Co., LTD | DongGuan Guangdong, China | Manufacturer, Repackager or relabeler | 1 | April 14, 2020 | 0 | 0 | 0 | api.fda.gov |
| Dongguan Yanxuan Biotechnology Co., Ltd | Dongguan City Guangdong, China | Manufacturer | 1 | May 9, 2025 | 0 | 0 | 0 | api.fda.gov |
| Nantong Health & Beyond Hygienic Products Inc. | Rugao City Jiangsu, China | Contract manufacturer, Manufacturer | 1 | May 18, 2021 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Guangdian Technology Co., Ltd | Shenzhen Guangdong, China | Manufacturer, Repackager or relabeler | 1 | April 14, 2020 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen The World Of Chamerlain Trade Lmport And Export Co.,ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | May 9, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Gel Word Medical Devices Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | September 9, 2025 | 0 | 0 | 0 | api.fda.gov |
| Boya Biotechnology Company Limited | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lvliang Lishi District Wenfeng Trade Co., Ltd. | Lvliang Shanxi, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yiwu Nianxun E-Commerce Co., Ltd. | Jinhua Zhejiang, China | Contract 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.