Shenzhen Kingboom Technology Co., Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Shenzhen Kingboom Technology Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Mar 2026. Active since 2025. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Kingboom Technology Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Shenzhen Reanny Medical Devices Management Consulting Co., Ltd. and Shenzhen Reanny Medical Devices Management Consulting Co.,.
2 devices