Cleared Traditional

ORTHODONTIC ARCH WIRE (K924805) - FDA 510(k) Clearance

Class I Dental device.

K924805 · Ultimate Wireforms, Inc. · Dental device
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Mar 1993
Decision
188d
Days
Class 1
Risk

K924805 is an FDA 510(k) clearance for the ORTHODONTIC ARCH WIRE. Classified as Wire, Orthodontic (product code DZC), Class I - General Controls.

Submitted by Ultimate Wireforms, Inc. (Terryville, US). The FDA issued a Cleared decision on March 31, 1993 after a review of 188 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.5410 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Ultimate Wireforms, Inc. devices

Submission Details

510(k) Number K924805 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 24, 1992
Decision Date March 31, 1993
Days to Decision 188 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
61d slower than avg
Panel avg: 127d · This submission: 188d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DZC Wire, Orthodontic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.5410
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.