Cleared Traditional

K062713 - ADHESIVE DC ACTIVATOR

K062713 is the FDA 510(k) clearance for ADHESIVE DC ACTIVATOR by Ivoclar Vivadent, Inc.. It is a Class 2 Dental device (product code KLE) cleared through the Traditional 510(k) pathway after a 52-day FDA review.

K062713 · Ivoclar Vivadent, Inc. · Dental device
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Nov 2006
Decision
52d
Days
Class 2
Risk

K062713 is an FDA 510(k) clearance for the ADHESIVE DC ACTIVATOR. Classified as Agent, Tooth Bonding, Resin (product code KLE), Class II - Special Controls.

Submitted by Ivoclar Vivadent, Inc. (Amherst, US). The FDA issued a Cleared decision on November 2, 2006 after a review of 52 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3200 - 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 Ivoclar Vivadent, Inc. devices

Submission Details

510(k) Number K062713 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 11, 2006
Decision Date November 02, 2006
Days to Decision 52 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
75d faster than avg
Panel avg: 127d · This submission: 52d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KLE Agent, Tooth Bonding, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3200
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 - KLE Agent, Tooth Bonding, Resin

All 248
Devices cleared under the same product code (KLE) and FDA review panel - the closest regulatory comparables to K062713.
PEAK SE, MODEL 5135
K063558 · Ultradent Products, Inc. · Dec 2006
PEAK BOND, MODEL 5133
K063557 · Ultradent Products, Inc. · Dec 2006
HKBOND 2006
K063062 · Heraeus Kulzer, Inc. · Dec 2006
PREMIER SELF-ETCHING BOND ENHANCER
K061998 · Premier Dental Products Co. · Oct 2006
CLEARFIL DC BOND
K062382 · Kuraray Medical, Inc. · Sep 2006
BOSWORTH DENTIN RESIN
K061611 · Harry J. Bosworth Co. · Sep 2006