Cleared Traditional

K001914 - CLEARFIL REPAIR

K001914 is an FDA 510(k) clearance for CLEARFIL REPAIR, manufactured by Kuraray Company, Ltd.. The device is a Class 2 Dental device with product code KLE cleared through the Traditional 510(k) pathway after a 48-day FDA review.

K001914 · Kuraray Company, Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2000
Decision
48d
Days
Class 2
Risk

K001914 is an FDA 510(k) clearance for the CLEARFIL REPAIR. Classified as Agent, Tooth Bonding, Resin (product code KLE), Class II - Special Controls.

Submitted by Kuraray Company, Ltd. (New York, US). The FDA issued a Cleared decision on August 10, 2000 after a review of 48 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 Kuraray Company, Ltd. devices

FDA 510(k) Submission Details - K001914

510(k) Number K001914 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 2000
Decision Date August 10, 2000
Days to Decision 48 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
79d faster than avg
Panel avg: 127d · This submission: 48d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KLE Device Classification - Class 2, Special Controls

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 347
Devices cleared under the same product code (KLE) and FDA review panel - the closest regulatory comparables to K001914.
SELF ETCH BONDING PRIMER
K003011 · Jeneric/Pentron, Inc. · Nov 2000
SOLOBOND PLUS
K003153 · Voco GmbH · Nov 2000
CERAM-PRIME
K002502 · S & C Polymer GmbH · Nov 2000
MODIFICATION TO PROMPT L-POP
K001494 · Espe Dental AG · Jul 2000
PQ1
K000189 · Ultradent Products, Inc. · May 2000
KERR GEL ETCHANT
K000954 · Sybron Dental Specialties, Inc. · Apr 2000