Cleared Traditional

K020253 - 4 ALL (DW286A)

K020253 is an FDA 510(k) clearance for 4 ALL (DW286A), manufactured by Ivoclar Vivadent, Inc.. The device is a Class 2 Dental device with product code EJH cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K020253 · Ivoclar Vivadent, Inc. · Dental device
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Apr 2002
Decision
83d
Days
Class 2
Risk

K020253 is an FDA 510(k) clearance for the 4 ALL (DW286A). Classified as Alloy, Metal, Base (product code EJH), Class II - Special Controls.

Submitted by Ivoclar Vivadent, Inc. (Amherst, US). The FDA issued a Cleared decision on April 17, 2002 after a review of 83 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3710 - 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 Ivoclar Vivadent, Inc. devices

FDA 510(k) Submission Details - K020253

510(k) Number K020253 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 24, 2002
Decision Date April 17, 2002
Days to Decision 83 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 faster than avg
Panel avg: 127d · This submission: 83d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJH Device Classification - Class 2, Special Controls

Product Code EJH Alloy, Metal, Base
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3710
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 - EJH Alloy, Metal, Base

All 99
Devices cleared under the same product code (EJH) and FDA review panel - the closest regulatory comparables to K020253.
CONTINUM
K040179 · Aalba Dent, Inc. · Mar 2004
VERASOFT ES
K033356 · Aalba Dent, Inc. · Dec 2003
KAVO EVEREST TITANBLANK
K024214 · Kavo America · Mar 2003
D.SIGN 15 (DW286 B)
K020898 · Ivoclar Vivadent, Inc. · Mar 2002
PISCES PLUS (DW286 C)
K020183 · Ivoclar Vivadent, Inc. · Mar 2002
D.SIGN 30
K010381 · Ivoclar North America, Inc. · Mar 2001