Wuhan Pioon Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Medical Diode Laser (UTU3-F7B,UTU3-F7W,UTU3-G7B,UTU3-G7W,UTU-G20B,UTU-G20W), Medical Diode Laser (Models: MZ-GK, MZ-K20, MZ-N75), Medical Diode Laser (M2-GK)
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Wuhan Pioon Technology Co., Ltd. General & Plastic Surgery ✕
6 devices
Cleared
Apr 04, 2025
Medical Diode Laser (Models: MZ-GK, MZ-K20, MZ-N75)
General & Plastic Surgery
30d
Cleared
Jun 17, 2024
Medical Diode Laser (M2-GK)
General & Plastic Surgery
90d
Cleared
Jun 10, 2024
Medical Diode Laser (S1Pro)
General & Plastic Surgery
95d
Cleared
Mar 21, 2024
Medical Diode Laser (Model: L2)
General & Plastic Surgery
58d
Cleared
Aug 03, 2023
Medical Diode Laser, Model S1Pro
General & Plastic Surgery
65d
Cleared
Mar 31, 2023
Medical Diode Laser (M2)
General & Plastic Surgery
58d