Cleared Traditional

K844325 - COE-LITE POLYMERIZATION UNIT

K844325 is the FDA 510(k) clearance for COE-LITE POLYMERIZATION UNIT by Coe Laboratories, Inc.. It is a Class 2 Dental device (product code EBZ) cleared through the Traditional 510(k) pathway after a 34-day FDA review.

K844325 · Coe Laboratories, Inc. · Dental device
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Dec 1984
Decision
34d
Days
Class 2
Risk

K844325 is an FDA 510(k) clearance for the COE-LITE POLYMERIZATION UNIT. Classified as Activator, Ultraviolet, For Polymerization (product code EBZ), Class II - Special Controls.

Submitted by Coe Laboratories, Inc. (Alsip, US). The FDA issued a Cleared decision on December 11, 1984 after a review of 34 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 Coe Laboratories, Inc. devices

Submission Details

510(k) Number K844325 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 07, 1984
Decision Date December 11, 1984
Days to Decision 34 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
93d faster than avg
Panel avg: 127d · This submission: 34d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 81
Devices cleared under the same product code (EBZ) and FDA review panel - the closest regulatory comparables to K844325.
TULUX-FILTER
K892517 · Espe GmbH (Us) · Aug 1989
KULZER TRANSLUX EC
K892456 · Kulzer, Inc. · Jun 1989
PHOTO-CURING LIGHT
K882145 · Dentsply Intl. · Sep 1988
TRANSLUX CL
K843823 · Kulzer, Inc. · Dec 1984
PRISMA III
K832320 · Dentsply Intl. · Aug 1983
KULZER TRANSLUX VISIBLE LIGHT CURING
K811668 · Kulzer, Inc. · Jul 1981