Cleared Abbreviated

K112044 - ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT MODEL 240XXX (U), MOCK-UP DIRECT FLOW MODEL 24A

K112044 is an FDA 510(k) clearance for ANAXBLEND MODEL 20XXX (SEVERAL), manufactured by Anaxdent GmbH. The device is a Class 2 Dental device with product code EBF cleared through the Abbreviated 510(k) pathway after a 192-day FDA review.

K112044 · Anaxdent GmbH · Dental device
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Jan 2012
Decision
192d
Days
Class 2
Risk

K112044 is an FDA 510(k) clearance for the ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT MODE.... Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Anaxdent GmbH (Tarpley, US). The FDA issued a Cleared decision on January 26, 2012 after a review of 192 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - the FDA dental device regulatory framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Anaxdent GmbH devices

FDA 510(k) Submission Details - K112044

510(k) Number K112044 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 18, 2011
Decision Date January 26, 2012
Days to Decision 192 days
Submission Type Abbreviated
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
65d slower than avg
Panel avg: 127d · This submission: 192d
Pathway characteristics
Standards-based clearance path.

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 711
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K112044.
CLEARFIL MAJESTY FLOW
K121583 · Kuraray Noritake Dental, Inc. · Jul 2012
ES FLOW
K120768 · Spident Co., Ltd. · May 2012
SPEE-DEE PATCH
K113617 · Pulpdent Corporation · Mar 2012
N-HYBRIDE-COMPOSITE LC FLOW
K113444 · Voco GmbH · Dec 2011
N-HYBRIDE-COMPOSITE LC
K113563 · Voco GmbH · Dec 2011
COMPONEER
K112168 · Coltene/Whaledent AG · Nov 2011