
H.B.M. USA Co.,Inc.
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MEDISPO (POWDERED) AND MEDISPO-PF (POWDER-FREE) SURGEONS GLOVE is an FDA 510(k)-cleared medical device (K050071) manufactured by H.B.M. USA Co.,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 10, 2005. Regulation: 8.