Data / Medical devices / China / Shenzhen Rongfeng Technology Co.,Ltd
Shenzhen Rongfeng Technology Co.,Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 2 510(k) clearances
Shenzhen Rongfeng Technology Co.,Ltd is registered with the FDA (registration 3029824200) in Shenzhen Guangdong, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 21, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3029824200
- Address
- 3/F, R Building, Shasi Industrial Park, Shajing Town, Baoan District, Shenzhen Guangdong, China, 518104
- Owner or operator
- Shenzhen Rongfeng Technology Co.,Ltd (10088733)
- Roles
- Manufacturer
- First device listed
- October 6, 2023
- Registered through
- 2026
- Brand names listed
- Digital Thermometer, Model: QT001, QT001-01, QT002, QT003, QT006, DT102, DT103, Infrared Thermometer, Model: IR8807, IR816, IR903, IR818, IR819, Tourniquet, Model: TQ01
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Continuous Measurement Thermometer | FLL | 2 | Manufacturer | accessdata.fda.gov |
| Tourniquet, Nonpneumatic | GAX | 1 | 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 |
|---|---|---|---|---|---|---|
| July 21, 2023 | K223037 | Infrared Thermometer, Model: IR8807 | FLL | Substantially Equivalent | Shen Zhen Rong Feng Technology Co., Ltd. | accessdata.fda.gov |
| May 10, 2023 | K223044 | Digital Thermometer (Model QT001) | FLL | Substantially Equivalent | Shen Zhen Rong Feng Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 21, 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.