Data / Medical devices / China / Wuhan Pioon Technology Co.,Ltd.
Wuhan Pioon Technology Co.,Ltd.: FDA-registered device maker in Wuhan Hubei, China, 2 510(k) clearances
Wuhan Pioon Technology Co.,Ltd. is registered with the FDA (registration 3015262665) in Wuhan Hubei, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated August 3, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015262665
- Address
- 12th Floor, Building 1, Innovative Unit, R&D Center Project, Marine World Shipyard Park No. 16 Fozuling 3rd Road, East Lake High-tech Development Zone, Wuhan Hubei, China, 430205
- Owner or operator
- Wuhan Pioon Technology Co,. Ltd. (10060271)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- April 18, 2019
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Contract manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 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 |
|---|---|---|---|---|---|---|
| August 3, 2023 | K231548 | Medical Diode Laser, Model S1Pro | GEX | Substantially Equivalent | Wuhan Pioon Technology Co., Ltd. | accessdata.fda.gov |
| March 31, 2023 | K230274 | Medical Diode Laser (M2) | GEX | Substantially Equivalent | Wuhan Pioon Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 3, 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.