Data / Medical devices / Protector, Hearing (Insert) / China
FDA-registered makers of Protector, Hearing (Insert) in China: 13 establishments
13 establishments in China are registered with the FDA to make Protector, Hearing (Insert) (product code EWD). 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
- Protector, Hearing (Insert)
- Product code
- EWD
- Country
- China
Makers of Protector, Hearing (Insert) in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ansico (xiamen) Optical Technology Co., Ltd. | Xiamen Fujian, China | Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.fda.gov | |
| Changzhou Recoo Healthcare Co., Ltd. | Changzhou Jiangsu, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cixi Bohong Bath Appliances Co., Ltd. | Ningbo Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong J&y Industrial Co., Ltd. | Guangzhou Guangdong, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangzhou Junyue Foam Earplug Co.,ltd. | GUANGZHOU CITY Guangdong, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hangzhou Greatstar Industrial Co., Ltd | Hangzhou Zhejiang, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Huizhou Gold Rose Technology Co.,ltd | huizhou Guangdong, China | Contract manufacturer, Exporter to the US, Foreign private label distributor, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Junhe Industry And Trade Co.,ltd | Yangjiang Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangyin Sian Plastic Protech Co., Ltd. | Jiangyin Jiangsu, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo R&m(rato) International Trading Co., Ltd. | NINBGO Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wuhan Jinshengyuan Textile Manufacturing Co Ltd. | Wuhan Hubei, China | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhejiang Baron Travel Products Co.,ltd | JINHUA CITY Zhejiang, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhejiang Longmed Medical Technology Co., Ltd. | Huzhou 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.