Dixi Medical is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Dixi Medical - FDA 510(k) Cleared Devices
Recent clearances: DIXI Medical Microdeep Micro-Macro Depth Electrodes, Dixi Medical Intraoperative Subdural Electrodes (Strips and Grids)
3
Total
3
Cleared
0
Denied
Dixi Medical has 3 FDA 510(k) cleared medical devices. Based in Chaudefontaine, FR.
Last cleared in 2021. Active since 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Dixi Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Domecus Consulting Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dixi Medical
3 devices