Shenzhen Kingboom Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Kingboom Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Electric nasal aspirator (BC027, BC030, BC033, BC035, BC035B), Electric nasal aspirator (BC026, BC025, BC023, BC028, BC029, BC036), Electric Nasal Aspirator (BC026, BC025, BC023)
3
Total
3
Cleared
0
Denied
Shenzhen Kingboom Technology Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: May 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.,.
FDA 510(k) Regulatory Record - Shenzhen Kingboom Technology Co., Ltd.
3 devices
Cleared
May 12, 2026
Electric nasal aspirator (BC027, BC030, BC033, BC035, BC035B)
Ear, Nose, Throat
89d
Cleared
Mar 13, 2026
Electric nasal aspirator (BC026, BC025, BC023, BC028, BC029, BC036)
Ear, Nose, Throat
52d
Cleared
Apr 23, 2025
Electric Nasal Aspirator (BC026, BC025, BC023)
Ear, Nose, Throat
47d