Medical Device Manufacturer · US , Tampa , FL

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

2 submissions · 2 cleared · Since 1998

Recent clearances: MAXISONIC FAMILY AND SWIFT ULTRASONIC SCALER, MRS-400, MAXI 400, MRSL-400, MAXI 400L

View 2 510(k) Devices ↓

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 . 176,325 total devices indexed.

Last updated: Sep 09, 2026