Cleared Traditional

K902893 - TI-CORE (DENTAL COMPOSITE)

K902893 is the FDA 510(k) clearance for TI-CORE (DENTAL COMPOSITE) by Medical Device Inspection Co., Inc.. It is a Class 2 Dental device (product code EBF) cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K902893 · Medical Device Inspection Co., Inc. · Dental device
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Sep 1990
Decision
66d
Days
Class 2
Risk

K902893 is an FDA 510(k) clearance for the TI-CORE (DENTAL COMPOSITE). Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Medical Device Inspection Co., Inc. (Great Neck, US). The FDA issued a Cleared decision on September 6, 1990 after a review of 66 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 Medical Device Inspection Co., Inc. devices

Submission Details

510(k) Number K902893 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 02, 1990
Decision Date September 06, 1990
Days to Decision 66 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
61d faster than avg
Panel avg: 127d · This submission: 66d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 578
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K902893.
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