D.B.I. America Corp.

D.B.I. America Corp. holds 2 FDA 510(k) medical device clearances, first cleared 1998, most recent 2005.

Top product codes for D.B.I. America Corp.

EFB — Dental1 device
ELC — Dental1 device

Recent clearances by D.B.I. America Corp.

K051910 — MAXISONIC FAMILY AND SWIFT ULTRASONIC SCALERCode ELC·2005-09-02
K981990 — MRS-400, MAXI 400, MRSL-400, MAXI 400LCode EFB·1998-06-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.