Kavo America Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kavo America Corporation - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Kavo America Corporation has 4 FDA 510(k) cleared medical devices. Based in Deer Field, US.
Historical record: 4 cleared submissions from 2003 to 2005. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Kavo America Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kavo America Corporation
4 devices