Medical Device Manufacturer · US , Tampa , FL

D.B.I. America Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - D.B.I. America Corp. Dental ✕

2 devices

1-2 of 2

Cleared Sep 02, 2005

MAXISONIC FAMILY AND SWIFT ULTRASONIC SCALER

Cleared Jun 22, 1998

MRS-400, MAXI 400, MRSL-400, MAXI 400L

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 28, 2026