Cleared Traditional

'E-Z FLOSS' AND 'LAZY FLOSS' (K860963) - FDA 510(k) Clearance

Class I Dental device.

K860963 · Login Industries , Ltd. · Dental device
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Mar 1986
Decision
13d
Days
Class 1
Risk

K860963 is an FDA 510(k) clearance for the 'E-Z FLOSS' AND 'LAZY FLOSS'. Classified as Floss, Dental (product code JES), Class I - General Controls.

Submitted by Login Industries , Ltd. (Canada, CA). The FDA issued a Cleared decision on March 26, 1986 after a review of 13 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6390 - 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 Login Industries , Ltd. devices

Submission Details

510(k) Number K860963 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 13, 1986
Decision Date March 26, 1986
Days to Decision 13 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
114d faster than avg
Panel avg: 127d · This submission: 13d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JES Floss, Dental
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.6390
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.