Shenzhen Wisonic Medical Technology Co. , Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Wisonic Medical Technology Co. , Ltd. - FDA 510(k) Cleared D...
Recent clearances: Carnation series Diagnostic Ultrasound System, Clivia series Diagnostic Ultrasound System, Labat series Diagnostic Ultrasound System
7
Total
7
Cleared
0
Denied
Shenzhen Wisonic Medical Technology Co. , Ltd. has 7 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Last cleared in 2023. Active since 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Wisonic Medical Technology Co. , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Guangzhou Osmunda Medical Device Technical Service Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Shenzhen Wisonic Medical Technology Co. , Ltd.
7 devices
Cleared
Sep 15, 2023
Carnation series Diagnostic Ultrasound System
Radiology
249d
Cleared
Dec 02, 2021
Clivia series Diagnostic Ultrasound System
Radiology
164d
Cleared
Jul 30, 2021
Labat series Diagnostic Ultrasound System
Radiology
190d
Cleared
Feb 07, 2020
Paragon XHD Diagnostic Ultrasound System
Radiology
263d
Cleared
Nov 20, 2018
Piloter Exp/Piloter/Piloter P Diagnostic Ultrasound System
Radiology
54d
Cleared
May 09, 2018
Navi e/Navi s/Navi X Diagnostic Ultrasound System
Radiology
78d
Cleared
Jan 02, 2018
Clover 50/Clover60/Clover70 Diagnostic Ultrasound System
Radiology
368d