Cleared Traditional

K963652 - PULPDENT DESENSITIZER

K963652 is an FDA 510(k) clearance for PULPDENT DESENSITIZER, manufactured by Pulpdent Corp.. The device is a Class 2 Dental device with product code EBF cleared through the Traditional 510(k) pathway after a 29-day FDA review.

K963652 · Pulpdent Corp. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1996
Decision
29d
Days
Class 2
Risk

K963652 is an FDA 510(k) clearance for the PULPDENT DESENSITIZER. 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 October 11, 1996 after a review of 29 days - a notably fast clearance cycle.

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: 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 Pulpdent Corp. devices

FDA 510(k) Submission Details - K963652

510(k) Number K963652 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 12, 1996
Decision Date October 11, 1996
Days to Decision 29 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
98d faster than avg
Panel avg: 127d · This submission: 29d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EBF Device Classification - Class 2, Special Controls

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 797
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K963652.
FIBREKOR
K964578 · Jeneric/Pentron, Inc. · Dec 1996
COJET SYSTEM
K963735 · Espe GmbH & Co. Kg. · Nov 1996
PRODIGY AC
K963805 · Sybron Dental Specialties, Inc. · Nov 1996
DENTAL PREP WASH AND PREP DISINFECT
K962909 · William J. Day · Oct 1996
TEAM ETCH
K963311 · Centrix, Inc. · Oct 1996
TARGIS SYSTEM
K962878 · Ivoclar North America, Inc. · Sep 1996