Vita is one of 25180 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vita - FDA 510(k) Cleared Devices
Recent clearances: VITA CAD-TEMP FOR INLAB, MODEL, VX59-4002, VX59-4010, VX59-4102, VX59-4110, VX59-4202, VX59-4210, VX59-4302, VX59-4310
1
Total
1
Cleared
0
Denied
Vita has 1 FDA 510(k) cleared medical devices. Based in Brea, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Vita Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vita
1 devices