Cleared Traditional

K031615 - SLED CURING LIGHT SYSTEM

K031615 is an FDA 510(k) clearance for SLED CURING LIGHT SYSTEM, manufactured by Dentsply International. The device is a Class 2 Dental device with product code EBZ cleared through the Traditional 510(k) pathway after a 59-day FDA review.

K031615 · Dentsply International · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2003
Decision
59d
Days
Class 2
Risk

K031615 is an FDA 510(k) clearance for the SLED CURING LIGHT SYSTEM. Classified as Activator, Ultraviolet, For Polymerization (product code EBZ), Class II - Special Controls.

Submitted by Dentsply International (York, US). The FDA issued a Cleared decision on July 21, 2003 after a review of 59 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6070 - 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 Dentsply International devices

FDA 510(k) Submission Details - K031615

510(k) Number K031615 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 23, 2003
Decision Date July 21, 2003
Days to Decision 59 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
69d faster than avg
Panel avg: 128d · This submission: 59d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBZ Device Classification - Class 2, Special Controls

Product Code EBZ Activator, Ultraviolet, For Polymerization
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.6070
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 - EBZ Activator, Ultraviolet, For Polymerization

All 177
Devices cleared under the same product code (EBZ) and FDA review panel - the closest regulatory comparables to K031615.
COLTOLUX LED CURING LIGHT
K040551 · Coltene/Whaledent, Inc. · Mar 2004
BLUEPHASE
K033520 · Ivoclar Vivadent, Inc. · Dec 2003
MINI L.E.D., MODEL: MINI L.E.D., MODEL SMARTLITE MINI
K032465 · Satelec · Oct 2003
RADII
K030568 · Southern Dental Industries, Inc. · Apr 2003
PALMLIGHT
K020057 · CAO Group, Inc. · Aug 2002
FLASH-LITE LED DENTAL CURING LIGHT
K022184 · Discus Dental, Inc. · Aug 2002