Cleared Traditional

K901913 - SYNTAC (DENTIN BONDING AGENT)

K901913 is the FDA 510(k) clearance for SYNTAC (DENTIN BONDING AGENT) by Ivoclar North America, Inc.. It is a Class 2 Dental device (product code KLE) cleared through the Traditional 510(k) pathway after a 61-day FDA review.

K901913 · Ivoclar North America, Inc. · Dental device
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Jun 1990
Decision
61d
Days
Class 2
Risk

K901913 is an FDA 510(k) clearance for the SYNTAC (DENTIN BONDING AGENT). Classified as Agent, Tooth Bonding, Resin (product code KLE), Class II - Special Controls.

Submitted by Ivoclar North America, Inc. (Amherst, US). The FDA issued a Cleared decision on June 26, 1990 after a review of 61 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 Ivoclar North America, Inc. devices

Submission Details

510(k) Number K901913 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 26, 1990
Decision Date June 26, 1990
Days to Decision 61 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 127d · This submission: 61d
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 282
Devices cleared under the same product code (KLE) and FDA review panel - the closest regulatory comparables to K901913.
DEGUFILL (TM) BOND
K902744 · Degussa AG · Aug 1990
DEGUFILL (R) BOND
K901870 · Degussa AG · Aug 1990
DEGUFILL (R) ADHESIVE
K901871 · Degussa AG · Aug 1990
PERTAC BOND
K900558 · Espe GmbH (Us) · Apr 1990
ALL-BOND DENTIN BONDING SYSTEM
K897020 · Bisco, Inc. · Mar 1990
9.6% HYDROFLUORIC ACID GEL
K896655 · Pulpdent Corp. · Feb 1990