
Handpiece Headquarters, Inc. - Hpr, Inc.
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HHC, SCORE, HENRY SCHEIN CANISTER HANDPIECE is an FDA 510(k)-cleared medical device (K080682) manufactured by Handpiece Headquarters, Inc. - Hpr, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 10, 2008. Regulation: 8.