Cleared Traditional

K010267 - PALFIQUE ESTELITE LV CLEAR

K010267 is an FDA 510(k) clearance for PALFIQUE ESTELITE LV CLEAR, manufactured by Tokuyama America, Inc.. The device is a Class 2 Dental device with product code EBF cleared through the Traditional 510(k) pathway after a 29-day FDA review.

K010267 · Tokuyama America, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2001
Decision
29d
Days
Class 2
Risk

K010267 is an FDA 510(k) clearance for the PALFIQUE ESTELITE LV CLEAR. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Tokuyama America, Inc. (Washington, US). The FDA issued a Cleared decision on February 27, 2001 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - 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 Tokuyama America, Inc. devices

FDA 510(k) Submission Details - K010267

510(k) Number K010267 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 29, 2001
Decision Date February 27, 2001
Days to Decision 29 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
98d faster than avg
Panel avg: 127d · This submission: 29d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBF Device Classification - Class 2, Special Controls

Product Code EBF Material, Tooth Shade, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3690
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 - EBF Material, Tooth Shade, Resin

All 670
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K010267.
3M ESPE HAUR
K010781 · 3M Company · Apr 2001
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TETRIC CERAM HB
K010250 · Ivoclar North America, Inc. · Feb 2001
PALFIQUE ESTELITE LV
K002863 · Tokuyama America, Inc. · Jan 2001
COLTENE AURA COMPOMER RESTORATIVE SYSTEM
K003034 · Coltene/Whaledent, Inc. · Nov 2000
RENEW LS-2
K003361 · Bisco, Inc. · Nov 2000