Data / Medical devices / China / Jinfeng Import & Export
Jinfeng Import & Export: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Jinfeng Import & Export is registered with the FDA (registration 3015781296) in Shenzhen Guangdong, China. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 22, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015781296
- Address
- RM419, Export Customs Building Of Wenjindu, Yanhe Road South, Luohu, District, Shenzhen Guangdong, China, 518002
- Owner or operator
- JINFENG IMPORT & EXPORT (10076712)
- Roles
- Exporter to the US
- First device listed
- September 9, 2020
- Registered through
- 2026
- Brand names listed
- Dragon Medical Occlusive Chest Seal, TRUE RESCUE
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Hydrophilic | NAC | 1 | Exporter to the US | accessdata.fda.gov |
| Dressing, Wound, Occlusive | NAD | 1 | Exporter to the US | accessdata.fda.gov |
| First Aid Kit Without Drug | OHO | 1 | Exporter to the US | accessdata.fda.gov |
| Mouthpiece, Breathing | BYP | 1 | Exporter to the US | accessdata.fda.gov |
| Valve, Non-Rebreathing | CBP | 2 | Exporter to the US | 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 22, 2010 | K083418 | CPR MASK | CBP | Substantially Equivalent | Firstar Healthcare Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Mouthpiece, Breathing
- All makers of Dressing, Wound, Hydrophilic
- All makers of First Aid Kit Without Drug
- All makers of Dressing, Wound, Occlusive
- All makers of Valve, Non-Rebreathing
Updated July 22, 2010. 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.