
Medishield, Inc.
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HMD-2000 BATTERY-POWERED MINI-DRILL, THE is an FDA 510(k)-cleared medical device (K780645) manufactured by Medishield, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 2, 1978. Regulation: 8.