K061664 is an FDA 510(k) clearance for the FORMCORE DC, MODEL 28-700100. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.
Submitted by J. Morita USA, Inc. (Irvine, US). The FDA issued a Cleared decision on September 8, 2006 after a review of 86 days - a notably fast clearance cycle.
This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - 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.
View all J. Morita USA, Inc. devices