Cleared Traditional

K062410 - CLEARFIL ESTHETIC CEMENT & DC BOND

K062410 is the FDA 510(k) clearance for CLEARFIL ESTHETIC CEMENT & DC BOND by Kuraray Medical, Inc.. It is a Class 2 Dental device (product code EMA) cleared through the Traditional 510(k) pathway after a 40-day FDA review.

K062410 · Kuraray Medical, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2006
Decision
40d
Days
Class 2
Risk

K062410 is an FDA 510(k) clearance for the CLEARFIL ESTHETIC CEMENT & DC BOND. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Kuraray Medical, Inc. (New York, US). The FDA issued a Cleared decision on September 26, 2006 after a review of 40 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3275 - 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 Kuraray Medical, Inc. devices

Submission Details

510(k) Number K062410 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 17, 2006
Decision Date September 26, 2006
Days to Decision 40 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
87d faster than avg
Panel avg: 127d · This submission: 40d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EMA Cement, Dental
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3275
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 - EMA Cement, Dental

All 253
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K062410.
GVC-100
K070840 · GC America, Inc. · May 2007
GC FUJI IX GP EXTRA
K070319 · GC America, Inc. · Feb 2007
MERON PLUS
K063554 · Voco GmbH · Jan 2007
MULTILINK SPRINT
K061781 · Ivoclar Vivadent, Inc. · Sep 2006
GC XLC-100 CAPSULE
K061535 · GC America, Inc. · Jul 2006
BISCEM TRANSLUCENT, BISCEM OPAQUE
K060701 · Bisco, Inc. · May 2006