Data / Medical devices / China / Joystar Electrical Appliances Manufacturing Co.,ltd.
Joystar Electrical Appliances Manufacturing Co.,ltd.: FDA-registered device maker in Foshan Guangdong, China, 2 510(k) clearances
Joystar Electrical Appliances Manufacturing Co.,ltd. is registered with the FDA (registration 3021544150) in Foshan Guangdong, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated March 9, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3021544150
- Address
- 7 Xingye Road, Tooling Town, Shapu, Jun'an, Shunde, Foshan Guangdong, China, 528329
- Owner or operator
- Joystar Electrical Appliances Manufacturing Co.,Ltd. (10087355)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- February 16, 2023
- Registered through
- 2026
- Brand names listed
- Momcozy Wearable Breast Pump ( M5);, Momcozy Wearable Electric Breast Pump (Model: S9 Pro, S12 Pro), Wearable Breast Pump: Model S10 (include S9 Pro/S12 Pro)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pump, Breast, Powered | HGX | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 9, 2023 | K223693 | Electric breast pump (model: M5) | HGX | Substantially Equivalent | Shenzhen Lutejiacheng Technology Co., Ltd. | accessdata.fda.gov |
| June 27, 2022 | K220309 | Wearable Breast Pump (Model S10) | HGX | Substantially Equivalent | Shenzhen Lutejiacheng Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated March 9, 2023. 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.