Cleared Traditional

K841111 - REMBRANDT SHADE MODIFICATION KIT

K841111 is the FDA 510(k) clearance for REMBRANDT SHADE MODIFICATION KIT by Den-Mat Corp.. It is a Class 2 Dental device (product code EBF) cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K841111 · Den-Mat Corp. · Dental device
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Mar 1984
Decision
15d
Days
Class 2
Risk

K841111 is an FDA 510(k) clearance for the REMBRANDT SHADE MODIFICATION KIT. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Den-Mat Corp. (Walker, US). The FDA issued a Cleared decision on March 30, 1984 after a review of 15 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - 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 Den-Mat Corp. devices

Submission Details

510(k) Number K841111 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 1984
Decision Date March 30, 1984
Days to Decision 15 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
112d faster than avg
Panel avg: 127d · This submission: 15d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EBF Material, Tooth Shade, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3690
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Dental devices follow this clearance model.

Regulatory Peers - EBF Material, Tooth Shade, Resin

All 578
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K841111.
LIGHT CURED RESIN BONDED CERAMIC
K833797 · 3M Company · Apr 1984
ESTIC MICROFILL
K840176 · Kulzer, Inc. · Apr 1984
PRE-LOADED C-R TUBES FOR SYRINGE
K833725 · Centrix, Inc. · Mar 1984
CURAY-MATCH PAINT-ON COMPOSITE RESTOR
K833810 · Scientific Pharmaceuticals, Inc. · Feb 1984
MATERIAL TOOTHSADE RESIN
K834247 · Scientific Pharmaceuticals, Inc. · Feb 1984
VISIO-GEM
K833757 · Espe GmbH (Us) · Feb 1984