Cleared Traditional

K905811 - ARGENCO 52HN

K905811 is the FDA 510(k) clearance for ARGENCO 52HN by Argen Precious Metals, Inc.. It is a Class 2 Dental device (product code EJT) cleared through the Traditional 510(k) pathway after a 32-day FDA review.

K905811 · Argen Precious Metals, Inc. · Dental device
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Jan 1991
Decision
32d
Days
Class 2
Risk

K905811 is an FDA 510(k) clearance for the ARGENCO 52HN. Classified as Alloy, Gold-based Noble Metal (product code EJT), Class II - Special Controls.

Submitted by Argen Precious Metals, Inc. (San Diego, US). The FDA issued a Cleared decision on January 29, 1991 after a review of 32 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3060 - 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 Argen Precious Metals, Inc. devices

Submission Details

510(k) Number K905811 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 28, 1990
Decision Date January 29, 1991
Days to Decision 32 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
95d faster than avg
Panel avg: 127d · This submission: 32d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EJT Alloy, Gold-based Noble Metal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3060
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 - EJT Alloy, Gold-based Noble Metal

All 377
Devices cleared under the same product code (EJT) and FDA review panel - the closest regulatory comparables to K905811.
MAXIGOLD
K905327 · Ivoclar North America, Inc. · Feb 1991
WILL-CERAM W
K905329 · Ivoclar North America, Inc. · Feb 1991
TYPE III DENTAL GOLD ALLOY FOR CROWN & BRIDGE APP.
K905761 · Argen Precious Metals, Inc. · Jan 1991
MIDIGOLD 50
K905322 · Ivoclar North America, Inc. · Jan 1991
VARIOUS
K905319 · Ivoclar North America, Inc. · Jan 1991
GDC-1501
K904695 · Deringer-Ney, Inc. · Jan 1991