Exini Diagnostics AB is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Exini Diagnostics AB - FDA 510(k) Cleared Devices
Recent clearances: aPROMISE X, aPROMISE, aBSI
4
Total
4
Cleared
0
Denied
Exini Diagnostics AB has 4 FDA 510(k) cleared medical devices. Based in Indianpolis, US.
Last cleared in 2022. Active since 2012. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Exini Diagnostics AB Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Biologics Consulting Group and Biologics Consulting.
FDA 510(k) Regulatory Record - Exini Diagnostics AB
4 devices