K790325 is an FDA 510(k) clearance for the REPRODENT. Classified as Resin, Denture, Relining, Repairing, Rebasing (product code EBI), Class II - Special Controls.
Submitted by Premier Dental Products Co. (Walker, US). The FDA issued a Cleared decision on March 2, 1979 after a review of 15 days - a notably fast clearance cycle.
This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3760 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.
Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.
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