
Gregory S. Jacob, D.D.S.
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PORTABLE LIGHT CURING UNIT is an FDA 510(k)-cleared medical device (K994048) manufactured by Gregory S. Jacob, D.D.S.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 12, 2000. Regulation: 8.