
D.B.I. America Corp.
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MRS-400, MAXI 400, MRSL-400, MAXI 400L is an FDA 510(k)-cleared medical device (K981990) manufactured by D.B.I. America Corp.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 21, 1998. Regulation: 8.