Shenzhen Desida Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Desida Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LED Light Therapy Mask (Models: T2, RLD10), Baby Nasal Aspirator (BN002), Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NASA606,NASA608,NASA610)
6
Total
6
Cleared
0
Denied
Shenzhen Desida Technology Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Mar 2026. Active since 2022. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Desida 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 Shenzhen CT Bio-Tech Co., Ltd..
FDA 510(k) Regulatory Record - Shenzhen Desida Technology Co., Ltd.
6 devices
Cleared
Mar 16, 2026
LED Light Therapy Mask (Models: T2, RLD10)
General & Plastic Surgery
88d
Cleared
Jun 06, 2025
Baby Nasal Aspirator (BN002)
Ear, Nose, Throat
28d
Cleared
May 16, 2025
Electric Nasal Aspirator...
Ear, Nose, Throat
137d
Cleared
Mar 20, 2024
Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA006, NASA008,...
Ear, Nose, Throat
100d
Cleared
Oct 21, 2022
Hair Removal Device (Model: IPL-D26, IPL-D19)
General & Plastic Surgery
137d
Cleared
Aug 31, 2022
IPL sapphire ice cooling hair remove device
General & Plastic Surgery
86d