Dia Imaging Analysis, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Dia Imaging Analysis, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LVivo Software Application, LVivo Seamless, LVivo Software Application
10
Total
10
Cleared
0
Denied
Dia Imaging Analysis, Ltd. has 10 FDA 510(k) cleared radiology devices. Based in Beer-Sheva, IL.
Latest FDA clearance: Mar 2025. Active since 2020.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Medicsense USA, LLC and Medicsense USA.
FDA 510(k) Regulatory Record - Dia Imaging Analysis, Ltd.
10 devices
Cleared
Mar 17, 2025
LVivo Software Application
Radiology
91d
Cleared
Mar 06, 2025
LVivo Seamless
Radiology
133d
Cleared
Mar 03, 2025
LVivo Software Application
Radiology
144d
Cleared
Oct 04, 2024
LVivo Software Application
Radiology
219d
Cleared
May 24, 2024
LVivo IQS
Radiology
64d
Cleared
Feb 01, 2023
LVivo IQS
Radiology
127d
Cleared
Dec 09, 2021
LVivo Seamless
Radiology
125d
Cleared
Feb 05, 2021
LVivo Software Application
Radiology
28d
Cleared
Sep 29, 2020
LVivo Seamless
Radiology
27d
Cleared
Jun 23, 2020
LVivo Software Application
Radiology
145d