Dentimax is one of 21756 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentimax - FDA 510(k) Cleared Devices
Recent clearances: DENTIMAX DIGITAL X-RAY IMAGING SYSTEM SENSOR SIZE 1, 2, DENTIMAX USB CONTROL BOX
1
Total
1
Cleared
0
Denied
Dentimax has 1 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dentimax Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dentimax
1 devices