D.B.I. America Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
D.B.I. America Corp. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
D.B.I. America Corp. has 2 FDA 510(k) cleared medical devices. Based in Tampa, US.
Historical record: 2 cleared submissions from 1998 to 2005. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by D.B.I. America Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - D.B.I. America Corp.
2 devices