Wuhan Pioon Technology Co., Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Wuhan Pioon Technology Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Wuhan, CN.
Latest FDA clearance: May 2025. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Wuhan Pioon Technology Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Wuhan Pioon Technology Co., Ltd.
7 devices
Cleared
May 08, 2025
Medical Diode Laser (UTU3-F7B,UTU3-F7W,UTU3-G7B,UTU3-G7W,UTU-G20B,UTU-G20W)
Dental
153d
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