Data / Medical devices / China / Qingdao Yasee Medical Device Co.,ltd.
Qingdao Yasee Medical Device Co.,ltd.: FDA-registered device maker in QINGDAO Shandong, China, 1 510(k) clearance
Qingdao Yasee Medical Device Co.,ltd. is registered with the FDA (registration 3018008670) in QINGDAO Shandong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 12, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018008670
- Address
- floor 2,building1,No,9Xiuyuan Road,HIGH-TECH INDUSTRIAL DEVELOPMENT ZONE, QINGDAO Shandong, China, 266112
- Owner or operator
- Qingdao Yasee Medical Device Co.,Ltd. (10086381)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- November 4, 2022
- Registered through
- 2026
- Brand names listed
- Infrared Forehead Thermometers, YASEE
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Continuous Measurement Thermometer | FLL | 2 | Manufacturer | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Contract 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 |
|---|---|---|---|---|---|---|
| September 12, 2022 | K220084 | Infrared Forehead Thermometer | FLL | Substantially Equivalent | Qingdao Yasee Medical Device Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Continuous Measurement Thermometer
Updated September 12, 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.