Shenzhen Qianyu Technology Co., Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Shenzhen Qianyu Technology Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Oct 2025. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Qianyu Technology Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Feiying Drug & Medical Consulting Technical Service Group and Guangzhou Tianke Testing Technology Service Co., Ltd..
6 devices
Cleared
Oct 17, 2025
JOVS Electric Stimulation Beauty Device (JE2)
Neurology
263d
Cleared
May 01, 2025
Wrinkle Treatment Device (JM1, JM2B)
General & Plastic Surgery
125d
Cleared
Apr 05, 2024
Wrinkle Treatment Device (JM2)
General & Plastic Surgery
59d
Cleared
Sep 07, 2023
IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9
General & Plastic Surgery
79d
Cleared
Apr 27, 2022
Hand-held IPL device (JOVS Hair Removal Device)
General & Plastic Surgery
54d
Cleared
Mar 28, 2022
Hand-held IPL device(JOVS Graphene Hair Removal Device)
General & Plastic Surgery
88d