Wuhan Pioon Technology Co., Ltd. is one of 2114 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Wuhan Pioon Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Medical Diode Laser (S1Pro+, S1Pro K15, S1Pro N6, S1Pro N75), 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)
8
Total
8
Cleared
0
Denied
Wuhan Pioon Technology Co., Ltd. has 8 FDA 510(k) cleared medical devices. Based in Wuhan, CN.
Latest FDA clearance: Sep 2026. 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.
510(k) submissions have been managed by leanRAQA as regulatory consultant.
FDA 510(k) Regulatory Record - Wuhan Pioon Technology Co., Ltd.
8 devices
Cleared
Sep 10, 2026
Medical Diode Laser (S1Pro+, S1Pro K15, S1Pro N6, S1Pro N75)
General & Plastic Surgery
56d
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