Cleared Traditional

K926074 - PULPDENT DENTAL BOND ENCHANCER

K926074 is the FDA 510(k) clearance for PULPDENT DENTAL BOND ENCHANCER by Pulpdent Corp.. It is a Class 2 Dental device (product code EBF) cleared through the Traditional 510(k) pathway after a 105-day FDA review.

K926074 · Pulpdent Corp. · Dental device
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Mar 1993
Decision
105d
Days
Class 2
Risk

K926074 is an FDA 510(k) clearance for the PULPDENT DENTAL BOND ENCHANCER. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Pulpdent Corp. (Watertown, US). The FDA issued a Cleared decision on March 16, 1993 after a review of 105 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Pulpdent Corp. devices

Submission Details

510(k) Number K926074 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 01, 1992
Decision Date March 16, 1993
Days to Decision 105 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
22d faster than avg
Panel avg: 127d · This submission: 105d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EBF Material, Tooth Shade, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3690
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 - EBF Material, Tooth Shade, Resin

All 577
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K926074.
DENTIN BONDING AGENT
K920533 · Confi-Dental Products Co. · May 1993
VIVALUX
K926556 · Ivoclar North America, Inc. · Apr 1993
CLIP
K926418 · Voco GmbH · Mar 1993
BISCO D/C RESINOMER
K924151 · Bisco, Inc. · Dec 1992
TRIAD INLAY COMPOSITE
K923236 · Dentsply Intl. · Sep 1992
COMPOSITE AND PORCELAIN POLISHING PASTE PROD. LINE
K921407 · Ultradent Products, Inc. · Sep 1992