Cleared Traditional

K111465 - COMPOTHIXO

K111465 is an FDA 510(k) clearance for COMPOTHIXO, manufactured by Kerrhawe SA. The device is a Class 1 Dental device with product code DZN cleared through the Traditional 510(k) pathway after a 426-day FDA review.

K111465 · Kerrhawe SA · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2012
Decision
426d
Days
Class 1
Risk

K111465 is an FDA 510(k) clearance for the COMPOTHIXO. Classified as Instruments, Dental Hand (product code DZN), Class I - General Controls.

Submitted by Kerrhawe SA (Orange, US). The FDA issued a Cleared decision on July 25, 2012 after a review of 426 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4565 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Dental submissions.

View all Kerrhawe SA devices

FDA 510(k) Submission Details - K111465

510(k) Number K111465 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 26, 2011
Decision Date July 25, 2012
Days to Decision 426 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
299d slower than avg
Panel avg: 127d · This submission: 426d
Pathway characteristics
Predicate-based equivalence.

DZN Device Classification - Class 1, General Controls

Product Code DZN Instruments, Dental Hand
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.4565
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - DZN Instruments, Dental Hand

All 9
Devices cleared under the same product code (DZN) and FDA review panel - the closest regulatory comparables to K111465.
CONTACT MOLAR BANDS AND CONTOUR STRIPS
K901919 · Ivoclar North America, Inc. · Jun 1990
CENTRIX PCR MOLAR MATRIX FORMS (BANDS)
K861581 · Centrix, Inc. · May 1986
DENTAL MATRIX BAND
K822094 · Dentsply Intl. · Aug 1982
COREFORM MOLDS
K801530 · Sybron Corp. · Jul 1980
HEMO-WEDGE
K790555 · Parker Laboratories, Inc. · Jan 1980
RUWA MATRIX STRIPS
K790599 · Howmedica Corp. · May 1979