
Nobelpharma USA, Inc.
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NOBELPHARMA DRILLING EQUIPMENT DEC 500 is an FDA 510(k)-cleared medical device (K905436) manufactured by Nobelpharma USA, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 3, 1991. Regulation: 8.