Cleared Traditional

K953527 - PERMUALUTE INDIRECT RESTORATIVE BONDING...

K953527 is the FDA 510(k) clearance for PERMUALUTE INDIRECT RESTORATIVE BONDING... by Ultradent Products, Inc.. It is a Class 2 Dental device (product code KLE) cleared through the Traditional 510(k) pathway after a 33-day FDA review.

K953527 · Ultradent Products, Inc. · Dental device
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Aug 1995
Decision
33d
Days
Class 2
Risk

K953527 is an FDA 510(k) clearance for the PERMUALUTE INDIRECT RESTORATIVE BONDING PRIMERS. Classified as Agent, Tooth Bonding, Resin (product code KLE), Class II - Special Controls.

Submitted by Ultradent Products, Inc. (South Jordan, US). The FDA issued a Cleared decision on August 29, 1995 after a review of 33 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3200 - 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 Ultradent Products, Inc. devices

Submission Details

510(k) Number K953527 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 27, 1995
Decision Date August 29, 1995
Days to Decision 33 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
94d faster than avg
Panel avg: 127d · This submission: 33d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KLE Agent, Tooth Bonding, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3200
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 - KLE Agent, Tooth Bonding, Resin

All 248
Devices cleared under the same product code (KLE) and FDA review panel - the closest regulatory comparables to K953527.
IMPERVA ENSURABOND
K953613 · Shofu Dental Corp. · Oct 1995
FUJI BOND LC
K953166 · GC America, Inc. · Sep 1995
BOND-IT DUAL CURE ACTIVATOR
K953859 · Jeneric/Pentron, Inc. · Sep 1995
MS EMULSION
K952123 · Parkell, Inc. · Jun 1995
ABOND
K952124 · Parkell, Inc. · Jun 1995
PRIME & BOND DIRECT COMPOSITE BONDING AGENT
K951864 · Dentsply Intl. · May 1995