Cleared Special

K032081 - KAVO EVEREST ZS-BLANK MODELS

K032081 is the FDA 510(k) clearance for KAVO EVEREST ZS-BLANK MODELS by Kavo America. It is a Class 2 Dental device (product code EIH) cleared through the Special 510(k) pathway after a 17-day FDA review.

K032081 · Kavo America · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2003
Decision
17d
Days
Class 2
Risk

K032081 is an FDA 510(k) clearance for the KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Kavo America (Deer Field, US). The FDA issued a Cleared decision on July 24, 2003 after a review of 17 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Kavo America devices

Submission Details

510(k) Number K032081 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 07, 2003
Decision Date July 24, 2003
Days to Decision 17 days
Submission Type Special
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
110d faster than avg
Panel avg: 127d · This submission: 17d
Pathway characteristics
Modification to existing cleared device.

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 268
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K032081.
CARRARA PRESS SYSTEM
K033667 · Dentsply Intl. · Jan 2004
PFZ PORCELAIN SYSTEM
K033553 · Dentsply Intl. · Dec 2003
VINTAGE AL
K032165 · Shofu Dental Corp. · Sep 2003
IMAGINE REFLEX
K031326 · Wieland Dental + Technik GmbH & Co. KG · Jun 2003
VITA IN-CERAM YZ CUBES FOR CEREC
K022996 · Vident · Oct 2002
CERCON CERAM S PORCELAIN
K022796 · Dentsply Intl. · Sep 2002