Not currently registered with FDA under this name

D.B.I. America Corp.

Tampa, FL, United States. Named as applicant on 2 dental 510(k) clearances between 1998 and 2005. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 21998–2005
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names D.B.I. America Corp. as the applicant.

Decided	510(k)	Device	Device type
2 Sep 2005	K051910	MAXISONIC FAMILY AND SWIFT ULTRASONIC SCALER	ELC Ultrasonic Scaler
22 Jun 1998	K981990	MRS-400, MAXI 400, MRSL-400, MAXI 400L	EFB Dental Air-Powered Handpiece

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.