Cleared Traditional

K001798 - DC TITAN

K001798 is an FDA 510(k) clearance for DC TITAN, manufactured by Austenal, Inc.. The device is a Class 2 Dental device with product code EJH cleared through the Traditional 510(k) pathway after a 47-day FDA review.

K001798 · Austenal, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2000
Decision
47d
Days
Class 2
Risk

K001798 is an FDA 510(k) clearance for the DC TITAN. Classified as Alloy, Metal, Base (product code EJH), Class II - Special Controls.

Submitted by Austenal, Inc. (Chicago, US). The FDA issued a Cleared decision on July 31, 2000 after a review of 47 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3710 - 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 Austenal, Inc. devices

FDA 510(k) Submission Details - K001798

510(k) Number K001798 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 14, 2000
Decision Date July 31, 2000
Days to Decision 47 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
80d faster than avg
Panel avg: 127d · This submission: 47d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJH Device Classification - Class 2, Special Controls

Product Code EJH Alloy, Metal, Base
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3710
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 - EJH Alloy, Metal, Base

All 98
Devices cleared under the same product code (EJH) and FDA review panel - the closest regulatory comparables to K001798.
AUROFILM NP
K003387 · Metalor Dental USA Corp. · Jan 2001
JEWEL CAST III
K003037 · Jeneric/Pentron, Inc. · Dec 2000
GOLD CORE II
K003039 · Jeneric/Pentron, Inc. · Dec 2000
CERADIUM V NON-PRECIOUS CERAMIC ALLOY
K993572 · Matech, Inc. · Dec 1999
HI BOND NON-PRECIOUS CERAMIC ALLOY
K992881 · Matech, Inc. · Nov 1999
P10 SPECIAL
K993344 · North American Alloys, Inc. · Nov 1999