Cleared Traditional

K143524 - Fiber Disks and Blocks (TRINIA)

K143524 is an FDA 510(k) clearance for Fiber Disks and Blocks (TRINIA), manufactured by Bicon, LLC. The device is a Class 2 Dental device with product code EBF cleared through the Traditional 510(k) pathway after a 172-day FDA review.

K143524 · Bicon, LLC · Dental device
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Jun 2015
Decision
172d
Days
Class 2
Risk

K143524 is an FDA 510(k) clearance for the Fiber Disks and Blocks (TRINIA). Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Bicon, LLC (Boston, US). The FDA issued a Cleared decision on June 2, 2015 after a review of 172 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K143524

510(k) Number K143524 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 12, 2014
Decision Date June 02, 2015
Days to Decision 172 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
44d slower than avg
Panel avg: 128d · This submission: 172d
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 863
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