Cleared Traditional

HELIOMAT (K802684) - FDA 510(k) Clearance

Class I Dental device.

K802684 · Vivadent (Usa), Inc. · Dental device
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Nov 1980
Decision
27d
Days
Class 1
Risk

K802684 is an FDA 510(k) clearance for the HELIOMAT. Classified as Light, Fiber Optic, Dental (product code EAY), Class I - General Controls.

Submitted by Vivadent (Usa), Inc. (Mchenry, US). The FDA issued a Cleared decision on November 24, 1980 after a review of 27 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4620 - 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 Vivadent (Usa), Inc. devices

Submission Details

510(k) Number K802684 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 28, 1980
Decision Date November 24, 1980
Days to Decision 27 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
100d faster than avg
Panel avg: 127d · This submission: 27d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EAY Light, Fiber Optic, Dental
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.4620
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.