Data / Medical devices / Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure / China
FDA-registered makers of Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure in China: 9 establishments
9 establishments in China are registered with the FDA to make Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure (product code PWA). 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
- Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure
- Product code
- PWA
- Country
- China
Makers of Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| B&a Precision Silicone Rubber (dongguan) Co., Ltd | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fansheng Technology (guangdong) Co., Ltd. | Zhongshan City Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gaboss International Limited | KOWLOON Xinjiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangxi Partner Home Co., Ltd. | Nanchang City Jiangxi, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rrdonnelley | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Rainbow Technology Co.,ltd | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Root Innovation Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Tokyun Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wuxi Phanpy Baby Products Co., Ltd. | WUXI Jiangsu, 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.