Cleared Traditional

K072622 - STANDOUT 2

K072622 is an FDA 510(k) clearance for STANDOUT 2, manufactured by Kerr Corp.. The device is a Class 2 Dental device with product code ELW cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K072622 · Kerr Corp. · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Dec 2007
Decision
78d
Days
Class 2
Risk

K072622 is an FDA 510(k) clearance for the STANDOUT 2. Classified as Material, Impression (product code ELW), Class II - Special Controls.

Submitted by Kerr Corp. (Orange, US). The FDA issued a Cleared decision on December 4, 2007 after a review of 78 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3660 - 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.

FDA 510(k) Submission Details - K072622

510(k) Number K072622 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 17, 2007
Decision Date December 04, 2007
Days to Decision 78 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
50d faster than avg
Panel avg: 128d · This submission: 78d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ELW Device Classification - Class 2, Special Controls

Product Code ELW Material, Impression
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3660
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 - ELW Material, Impression

All 375
Devices cleared under the same product code (ELW) and FDA review panel - the closest regulatory comparables to K072622.
SYSTEM PLUS
K073475 · Continental Dental Laboratory · Mar 2008
ELITE GLASS
K073005 · Zhermack S.P.A. · Dec 2007
BISICO IMPRESSION SILICONES & ALGINATES
K072577 · Bisico GmbH & CO KG · Dec 2007
EMULATE ADVANCED
K072245 · Cavex Holland BV · Nov 2007
BLUGOO HD
K071192 · Lancer Orthodontics, Inc. · Jun 2007
COLORISE
K070677 · Zhermack S.P.A. · May 2007
K072622 · STANDOUT 2
Download PDF FDA Summary Kerr Corp.