D.B.I. America Corp. is one of 7767 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
Recent clearances: MRS-400, MAXI 400, MRSL-400, MAXI 400L
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.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - D.B.I. America Corp.
2 devices