Data / Medical devices / China / Cixi Ruihong Electric Appliance Co.,ltd.
Cixi Ruihong Electric Appliance Co.,ltd.: FDA-registered device maker in Ningbo Zhejiang, China, 2 510(k) clearances
Cixi Ruihong Electric Appliance Co.,ltd. is registered with the FDA (registration 3013699454) in Ningbo Zhejiang, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 3, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013699454
- Address
- No. 18, Xiamaojia Road, Shuangqingpu Village, Xinpu Town, Cixi, Ningbo Zhejiang, China, 315322
- Owner or operator
- Cixi Ruihong Electric Appliance Co.,Ltd. (10056322)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- November 28, 2017
- Registered through
- 2026
- Brand names listed
- Breast pump, Electric breast pump (Model: RH-228 , RH-338), RH668 Wearable Single Breast Pump, RH701 Wearable Breast Pump, RH702 Wearable Breast Pump, RH707 Wearable Breast Pump, RH708 Wearable Breast Pump, RH718 Wearable Breast Pump and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pump, Breast, Non-Powered | HGY | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Pump, Breast, Powered | HGX | 2 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| April 3, 2026 | K252744 | Wearable Electric Breast Pump (RH 668, RH 708, RH 718, RH 728) | HGX | Substantially Equivalent | Cixi Ruihong Electric Appliance Co., Ltd. | accessdata.fda.gov |
| April 9, 2021 | K201903 | Electric breast pump (Models: RH-228 and RH-338) | HGX | Substantially Equivalent | Cixi Ruihong Electric Appliance Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated April 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.