Cleared Traditional

K000951 - LUXAFORM

K000951 is an FDA 510(k) clearance for LUXAFORM, manufactured by Dmg USA, Inc.. The device is a Class 2 Dental device with product code EBG cleared through the Traditional 510(k) pathway after a 13-day FDA review.

K000951 · Dmg USA, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2000
Decision
13d
Days
Class 2
Risk

K000951 is an FDA 510(k) clearance for the LUXAFORM. Classified as Crown And Bridge, Temporary, Resin (product code EBG), Class II - Special Controls.

Submitted by Dmg USA, Inc. (Ayer, US). The FDA issued a Cleared decision on April 5, 2000 after a review of 13 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3770 - 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 Dmg USA, Inc. devices

FDA 510(k) Submission Details - K000951

510(k) Number K000951 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 23, 2000
Decision Date April 05, 2000
Days to Decision 13 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
114d faster than avg
Panel avg: 127d · This submission: 13d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBG Device Classification - Class 2, Special Controls

Product Code EBG Crown And Bridge, Temporary, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3770
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 - EBG Crown And Bridge, Temporary, Resin

All 117
Devices cleared under the same product code (EBG) and FDA review panel - the closest regulatory comparables to K000951.
FERMIT N PLUS
K003377 · Ivoclar North America, Inc. · Dec 2000
PROTEMP H
K002364 · Espe Dental AG · Aug 2000
3M QUIK TEMP TEMPORIZATION MATERIAL
K001114 · 3M Company · Jun 2000
JELTEMP
K991564 · J.F. Jelenko & Co., Inc. · Jun 1999
SMARTEMP
K991270 · Parkell, Inc. · May 1999
HIGH VISCOSITY COMPOSITE TEMPORARY (PROVISIONAL) MATERIAL
K980799 · Cosmedent, Inc. · Oct 1998