Data / Medical devices / Pump, Portable, Aspiration (Manual Or Powered) / China
FDA-registered makers of Pump, Portable, Aspiration (Manual Or Powered) in China: 12 establishments
12 establishments in China are registered with the FDA to make Pump, Portable, Aspiration (Manual Or Powered) (product code BTA). 10 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Pump, Portable, Aspiration (Manual Or Powered)
- Product code
- BTA
- Country
- China
Makers of Pump, Portable, Aspiration (Manual Or Powered) in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Shenzhen Kingboom Technology Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 3 | May 12, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Root Innovation Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 3 | May 26, 2026 | 0 | 0 | 0 | api.fda.gov |
| Laerdal Medical (suzhou) Co., Ltd. | 215009 Suzhou Jiangsu Province, China | Manufacturer | 2 | December 20, 1999 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Desida Technology Co., Ltd. | Shenzhen Guangdong, China | Contract manufacturer, Manufacturer | 2 | May 16, 2025 | 0 | 0 | 0 | api.fda.gov |
| Avita (wujiang) Co., Ltd | Wujiang City Jiangsu, China | Contract manufacturer, Manufacturer | 1 | May 26, 2010 | 0 | 0 | 0 | api.fda.gov |
| Hetaida Technology Co., Ltd. | Dongguan Guangdong, China | Manufacturer | 1 | July 1, 2024 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Dongjiang Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | April 14, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Hugemed Medical Technical Development Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 1 | May 14, 2026 | 0 | 0 | 0 | api.fda.gov |
| Zhongshan A&j Medical Equipment Co., Ltd. | Guangdong, China | Manufacturer | 1 | June 26, 2007 | 0 | 0 | 0 | api.fda.gov |
| Zhongshan GL Electronics Co.,ltd | ZHONGSHAN Guangdong, China | Manufacturer | 1 | October 7, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Bi-Rich Medical Devices Co., Ltd | Shenzhen City Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vincent Medical (dong Guan) Manufacturing Co., Ltd. | Dong Guan City Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.