Data / Medical devices / China / Guangzhou Yongyi Industrial Co., Ltd.
Guangzhou Yongyi Industrial Co., Ltd.: FDA-registered device maker in Guangzhou Guangdong, China, 2 510(k) clearances
Guangzhou Yongyi Industrial Co., Ltd. is registered with the FDA (registration 3016562061) in Guangzhou Guangdong, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 26, 2023. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3016562061
- Address
- Room #101/#201/#301,No.4, Majun Street, Nansha District, Guangzhou Guangdong, China, 511475
- Owner or operator
- Guangzhou Yongyi Industrial Co., Ltd. (10074414)
- Roles
- Manufacturer
- First device listed
- May 23, 2020
- Registered through
- 2026
- Brand names listed
- Dr. Brown's Digital Electric Breast Pump (models: BF103, BF100), Electric Breast Pumps (Models: YY-A46, YY-A203, YY-A204, YY-TC201), Kidro Digital Electric Breast Pump (models: YY-A11, YY-A21, YY-A31, YY-A41, YY-A51, YY-A103, YY-A104), Manual Breast Pump with Silicone Shield (YY-H61)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pump, Breast, Non-Powered | HGY | 1 | Manufacturer | accessdata.fda.gov |
| Pump, Breast, Powered | HGX | 2 | 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 |
|---|---|---|---|---|---|---|
| May 26, 2023 | K223329 | Electric Breast Pump (model: YY-A46, YY-A203, YY-A204, YY-TC201) | HGX | Substantially Equivalent | Guangzhou Yongyi Industrial Co., Ltd. | accessdata.fda.gov |
| March 30, 2020 | K192640 | Kidro Digital Electric Breast Pump, Dr. Brown's Digital Electric Breast Pump | HGX | Substantially Equivalent | Guangzhou Yongyi Industrial Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated May 26, 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.