Cleared Traditional

K133824 - CERASMART

K133824 is an FDA 510(k) clearance for CERASMART, manufactured by GC America, Inc.. The device is a Class 2 Dental device with product code EBF cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K133824 · GC America, Inc. · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Mar 2014
Decision
87d
Days
Class 2
Risk

K133824 is an FDA 510(k) clearance for the CERASMART. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by GC America, Inc. (Alsip, US). The FDA issued a Cleared decision on March 14, 2014 after a review of 87 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.

FDA 510(k) Submission Details - K133824

510(k) Number K133824 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 17, 2013
Decision Date March 14, 2014
Days to Decision 87 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 128d · This submission: 87d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBF Device Classification - Class 2, Special Controls

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 878
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K133824.
FILTEK BULK FILL POSTERIOR RESTROATIVE
K141081 · 3M Espe Dental Products · May 2014
HTFX-222
K133182 · GC America, Inc. · Apr 2014
TRINIA
K133608 · Bicon, LLC · Mar 2014
BEAUTIFIL E POSTERIOR, BEAUTIFIL BULK
K132748 · Shofu Dental Corporation · Dec 2013
MERIDIAN
K131753 · Ab Ardent · Nov 2013
BEAUTIFIL BULK FLOWABLE
K132141 · Shofu Dental Corporation · Oct 2013
K133824 · CERASMART
Download PDF FDA Summary GC America, Inc.