Data / Medical devices / China / Dongguan Rongfeng Medical Co.,ltd
Dongguan Rongfeng Medical Co.,ltd: FDA-registered device maker in Dongguan Guangdong, China, 1 510(k) clearance
Dongguan Rongfeng Medical Co.,ltd is registered with the FDA (registration 3016693518) in Dongguan Guangdong, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 20, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016693518
- Address
- Room 704, Building 1, No. 762 Xiecao Road Xiegang Town, Dongguan Guangdong, China, 523590
- Owner or operator
- Dongguan Rongfeng Medical Co.,Ltd (10075055)
- Roles
- Manufacturer
- First device listed
- June 5, 2020
- Registered through
- 2026
- Brand names listed
- Electric breast pump Wearable models EB29.EB50.EB51.EB52.EB53.EB60;H9.H10.H11.K8., Electric breast pump Wearable models GLE9.GLE10.GLE11.GLE21.GLE33.H13.H15.H16., Forehead temperature gun RT-105, baby electric nasal aspirator with models DQ21,DQ22,DQ22-PLUS, DQ22-PRO,DQ26,DQ23,DQ8,DQ25,DQ55, temperature gun RT-108
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bottle, Collection, Vacuum | KDQ | 2 | Manufacturer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | 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 |
|---|---|---|---|---|---|---|
| January 20, 2022 | K212884 | Electric breast pump | HGX | Substantially Equivalent | Dongguan Rongfeng Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Continuous Measurement Thermometer
- All makers of Pump, Breast, Powered
- All makers of Bottle, Collection, Vacuum
Updated January 20, 2022. 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.