Cleared Traditional

K072569 - METOXIT CAM-BLANKS

K072569 is an FDA 510(k) clearance for METOXIT CAM-BLANKS, manufactured by Metoxit AG. The device is a Class 2 Dental device with product code EIH cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K072569 · Metoxit AG · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2007
Decision
49d
Days
Class 2
Risk

K072569 is an FDA 510(k) clearance for the METOXIT CAM-BLANKS. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Metoxit AG (Austin, US). The FDA issued a Cleared decision on October 31, 2007 after a review of 49 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 Metoxit AG devices

FDA 510(k) Submission Details - K072569

510(k) Number K072569 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 12, 2007
Decision Date October 31, 2007
Days to Decision 49 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
78d faster than avg
Panel avg: 127d · This submission: 49d
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 288
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K072569.
VINTAGE ART
K080834 · Shofu Dental Corp. · Jun 2008
DENTAL CERAMIC
K080479 · Dmg USA, Inc. · May 2008
ZENO ZR DISC
K073108 · Wieland Dental + Technik GmbH & Co. KG · Nov 2007
IPS INLINE POM SYSTEM
K071848 · Ivoclar Vivadent, Inc. · Aug 2007
GC-ZIRCONIA
K071674 · GC America, Inc. · Aug 2007
PRESSX ZR
K070772 · Wieland Dental + Technik GmbH & Co. KG · Apr 2007