
Beavers Dental, Div. Sybron Canada, Ltd.
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BEAVERS' DENTAL DIAMOND INSTRUMENTS is an FDA 510(k)-cleared medical device (K880179) manufactured by Beavers Dental, Div. Sybron Canada, Ltd.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 8, 1988. Regulation: 8.