Cleared Traditional

K992067 - BELLEGLAZE

K992067 is an FDA 510(k) clearance for BELLEGLAZE, manufactured by Kerr Dental Materials Center. The device is a Class 2 Dental device with product code EBD cleared through the Traditional 510(k) pathway after a 70-day FDA review.

K992067 · Kerr Dental Materials Center · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1999
Decision
70d
Days
Class 2
Risk

K992067 is an FDA 510(k) clearance for the BELLEGLAZE. Classified as Coating, Filling Material, Resin (product code EBD), Class II - Special Controls.

Submitted by Kerr Dental Materials Center (Orange, US). The FDA issued a Cleared decision on August 27, 1999 after a review of 70 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3310 - 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 Kerr Dental Materials Center devices

FDA 510(k) Submission Details - K992067

510(k) Number K992067 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 18, 1999
Decision Date August 27, 1999
Days to Decision 70 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
57d faster than avg
Panel avg: 127d · This submission: 70d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBD Device Classification - Class 2, Special Controls

Product Code EBD Coating, Filling Material, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3310
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 - EBD Coating, Filling Material, Resin

All 42
Devices cleared under the same product code (EBD) and FDA review panel - the closest regulatory comparables to K992067.
UNINHIBITED
K021503 · Bisco, Inc. · Aug 2002
GINDA GUARD
K011239 · Cosmedent, Inc. · Feb 2002
LUXAGLAZE
K013179 · Dmg USA, Inc. · Oct 2001
FLOWABLE HYBRID
K980298 · Cosmedent, Inc. · Mar 1998
RENAMEL FLOWABLE COMPOSITE
K974494 · Cosmedent, Inc. · Feb 1998
NO-STICK COMPOSITE INSTRUMENT DIP
K901050 · Pulpdent Corp. · Apr 1990