Data / Medical devices / Device, Anti-Snoring / China
FDA-registered makers of Device, Anti-Snoring in China: 8 establishments
8 establishments in China are registered with the FDA to make Device, Anti-Snoring (product code LRK). 6 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
- Device, Anti-Snoring
- Product code
- LRK
- Country
- China
Makers of Device, Anti-Snoring in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Digital Dental Depot | zhuhai Guangdong, China | Exporter to the US, Manufacturer | 3 | June 11, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Sany Pioneer Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 3 | August 27, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Kesite Digital Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 2 | September 18, 2023 | 0 | 0 | 0 | api.fda.gov |
| Dongguan Yiyao Science & Technology Development Co., Ltd. | Dongguan City Guangdong, China | Contract manufacturer, Manufacturer | 1 | October 3, 2025 | 0 | 0 | 0 | api.fda.gov |
| Xiamen Yizhou Imp. & Exp. Co., Ltd. | Xiamen Fujian, China | Contract manufacturer, Exporter to the US | 1 | November 23, 2020 | 0 | 0 | 0 | api.fda.gov |
| Zhuhai DS Dental Technology Co., Ltd | Zhuhai Guangdong, China | Manufacturer | 1 | April 5, 2013 | 0 | 0 | 0 | api.fda.gov |
| Dongyang City Yonoel Outdoor Products Co.,ltd | Dongyang Zhejiang, China | Exporter to the US, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Modern Dental Laboratory (DG) Co., Ltd. | Dongguan Guangdong, 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.