Cleared Traditional

K092572 - CORE*IT DUAL

K092572 is an FDA 510(k) clearance for CORE*IT DUAL, manufactured by Spident Co., Ltd.. The device is a Class 2 Dental device with product code EBF cleared through the Traditional 510(k) pathway after a 5-day FDA review.

K092572 · Spident Co., Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2009
Decision
5d
Days
Class 2
Risk

K092572 is an FDA 510(k) clearance for the CORE*IT DUAL. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Spident Co., Ltd. (Incheon, KR). The FDA issued a Cleared decision on August 26, 2009 after a review of 5 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 Spident Co., Ltd. devices

FDA 510(k) Submission Details - K092572

510(k) Number K092572 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 21, 2009
Decision Date August 26, 2009
Days to Decision 5 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Regulatory Context
Review time vs. panel average
122d faster than avg
Panel avg: 127d · This submission: 5d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

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 646
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K092572.
COSMEDENT BRUSHABLE COMPOSITE
K092730 · Cosmedent, Inc. · Nov 2009
CLEARFIL MAJESTY POSTERIOR PLT
K092281 · Kuraray Medical, Inc. · Oct 2009
SONICFILL 2010
K091091 · Sybron Dental Specialties, Inc. · Oct 2009
GCUC-505
K091388 · GC America, Inc. · Jul 2009
MULTILINK IMPLANT
K090704 · Ivoclar Vivadent, Inc. · Jun 2009
AMARIS GINGIVA OPAQUER
K090843 · Voco GmbH · Jun 2009