Data / Medical devices / Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure
Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure (PWA): 21 FDA-registered makers in 9 countries
21 establishments in 9 countries are registered with the FDA to make Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure (product code PWA, Class 1, 21 CFR 884.5150). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- PWA
- Device class
- 1
- Regulation
- 884.5150
- Medical specialty
- Obstetrics/Gynecology
Makers by country
| Country | Makers |
|---|---|
| China | 9 |
| United States | 4 |
| Taiwan | 2 |
| India | 1 |
| Australia | 1 |
| Singapore | 1 |
| New Zealand | 1 |
| Malaysia | 1 |
| South Korea | 1 |
Makers of Breast Pump Accessory, Milk Expression Aid, Via Positive Pressure
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Acute Ideas Co., Ltd. | Taipei, Taiwan | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| B&a Precision Silicone Rubber (dongguan) Co., Ltd | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Better Babies LLC | Newport Beach, CA, United States | 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 | |
| Heuer International (A division of GST Corporation Limited) | NOIDA Uttar Pradesh, India | Foreign private label distributor, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Icon Plastics Pty Ltd | Hallam Victoria, Australia | 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 | |
| Jabil Circuit (Singapore) Pte Ltd | Singapore Central Singapore, Singapore | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medela LLC | Mchenry, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Munchkin Inc. | Van Nuys, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Maymom Taiwan Corp. LTD | Zhunan Township Miaoli, Taiwan | Complaint file establishment, 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 | |
| Think Green Limited | Kumeu Auckland, New Zealand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Toa Tec (M) SDN BHD | Malaysia Johor, Malaysia | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Unimom Co. | Osan-si Gyeonggi, South Korea | Exporter to the US, 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 | |
| Willow Innovations Inc. | Mountain View, CA, United States | Manufacturer, Specification developer | 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.