Cleared Traditional

K970045 - SOLARO 33

K970045 is the FDA 510(k) clearance for SOLARO 33 by Metalor Dental USA Corp.. It is a Class 2 Dental device (product code EJS) cleared through the Traditional 510(k) pathway after a 58-day FDA review.

K970045 · Metalor Dental USA Corp. · Dental device
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Mar 1997
Decision
58d
Days
Class 2
Risk

K970045 is an FDA 510(k) clearance for the SOLARO 33. Classified as Alloy, Other Noble Metal (product code EJS), Class II - Special Controls.

Submitted by Metalor Dental USA Corp. (North Attleborough, US). The FDA issued a Cleared decision on March 5, 1997 after a review of 58 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 Metalor Dental USA Corp. devices

Submission Details

510(k) Number K970045 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 06, 1997
Decision Date March 05, 1997
Days to Decision 58 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
69d faster than avg
Panel avg: 127d · This submission: 58d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EJS Alloy, Other 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 - EJS Alloy, Other Noble Metal

All 117
Devices cleared under the same product code (EJS) and FDA review panel - the closest regulatory comparables to K970045.
SILCAST (CODE NAME RD-0118)
K981247 · J.F. Jelenko & Co., Inc. · Jul 1998
V-DELTA 450
K972683 · Metalor Dental USA Corp. · Aug 1997
AUROFLUID 22
K970044 · Metalor Dental USA Corp. · Mar 1997
SOLDER GPY
K964705 · Gateway Alloys, Inc. · Dec 1996
SOLDER 650
K964706 · Gateway Alloys, Inc. · Dec 1996
SOLDER 585
K964707 · Gateway Alloys, Inc. · Dec 1996