Cleared Traditional

K993488 - LIGHT-CORE

K993488 is the FDA 510(k) clearance for LIGHT-CORE by Bisco, Inc.. It is a Class 2 Dental device (product code EBF) cleared through the Traditional 510(k) pathway after a 26-day FDA review.

K993488 · Bisco, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1999
Decision
26d
Days
Class 2
Risk

K993488 is an FDA 510(k) clearance for the LIGHT-CORE. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Bisco, Inc. (Schaumburg, US). The FDA issued a Cleared decision on November 10, 1999 after a review of 26 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 Bisco, Inc. devices

Submission Details

510(k) Number K993488 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 15, 1999
Decision Date November 10, 1999
Days to Decision 26 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
101d faster than avg
Panel avg: 127d · This submission: 26d
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 516
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K993488.
PA GEL 35% IN BLUE AND PA GEL 10% IN GREEN OR BLUE
K993716 · Harry J. Bosworth Co. · Dec 1999
PRE-VISION FILL
K993602 · Heraeus Kulzer, Inc. · Dec 1999
TETRIC FLOW
K993783 · Ivoclar North America, Inc. · Dec 1999
ILLUSION
K993192 · Bisco, Inc. · Oct 1999
POST CEMENT HI-X
K992248 · Bisco, Inc. · Aug 1999
PRODIGY 4 TRANSLUCENT SHADES
K992118 · Sybron Dental Specialties, Inc. · Aug 1999