Cleared Traditional

K063511 - CERAMILL ZI

K063511 is an FDA 510(k) clearance for CERAMILL ZI, manufactured by Amann Girrbach America, Inc.. The device is a Class 2 Dental device with product code EIH cleared through the Traditional 510(k) pathway after a 74-day FDA review.

K063511 · Amann Girrbach America, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2007
Decision
74d
Days
Class 2
Risk

K063511 is an FDA 510(k) clearance for the CERAMILL ZI. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Amann Girrbach America, Inc. (Deer Field, US). The FDA issued a Cleared decision on February 2, 2007 after a review of 74 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 Amann Girrbach America, Inc. devices

FDA 510(k) Submission Details - K063511

510(k) Number K063511 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 20, 2006
Decision Date February 02, 2007
Days to Decision 74 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 127d · This submission: 74d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EIH Device Classification - Class 2, Special Controls

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 325
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K063511.
GC-ZIRCONIA
K071674 · GC America, Inc. · Aug 2007
PRESSX ZR
K070772 · Wieland Dental + Technik GmbH & Co. KG · Apr 2007
CREATION CP-ZI PORCELAIN
K070114 · Jensen Industries, Inc. · Mar 2007
CARRARA VOLUMIA
K070019 · Dentsply Intl. · Jan 2007
INCORIS ZI
K062509 · Sirona Dental Systems GmbH · Sep 2006
INCORIS AL
K062506 · Sirona Dental Systems GmbH · Sep 2006