Wuhan Pioon Technology Co., Ltd.
Wuhan Pioon Technology Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2023, most recent 2026.
Top product codes for Wuhan Pioon Technology Co., Ltd.
Recent clearances by Wuhan Pioon Technology Co., Ltd.
- K262426 — Medical Diode Laser (S1Pro+, S1Pro K15, S1Pro N6, S1Pro N75)
- K243764 — Medical Diode Laser (UTU3-F7B,UTU3-F7W,UTU3-G7B,UTU3-G7W,UTU-G20B,UTU-G20W)
- K250656 — Medical Diode Laser (Models: MZ-GK, MZ-K20, MZ-N75)
- K240747 — Medical Diode Laser (M2-GK)
- K240644 — Medical Diode Laser (S1Pro)
- K240179 — Medical Diode Laser (Model: L2)
- K231548 — Medical Diode Laser, Model S1Pro
- K230274 — Medical Diode Laser (M2)
Data sourced from openFDA. This site is unofficial and independent of the FDA.