Cleared Traditional

K123952 - CEREC BLOCS C IN

K123952 is the FDA 510(k) clearance for CEREC BLOCS C IN by Sirona Dental Systems GmbH. It is a Class 2 Dental device (product code EIH) cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K123952 · Sirona Dental Systems GmbH · Dental device
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Mar 2013
Decision
89d
Days
Class 2
Risk

K123952 is an FDA 510(k) clearance for the CEREC BLOCS C IN. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Sirona Dental Systems GmbH (Bensheim, DE). The FDA issued a Cleared decision on March 20, 2013 after a review of 89 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6660 - 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 Sirona Dental Systems GmbH devices

Submission Details

510(k) Number K123952 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 21, 2012
Decision Date March 20, 2013
Days to Decision 89 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
38d faster than avg
Panel avg: 127d · This submission: 89d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EIH Powder, Porcelain
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.6660
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 - EIH Powder, Porcelain

All 272
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K123952.
VINTAGE MP PRESS OVER
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