Cleared Traditional

K913724 - SONEX ULTRASONIC TOOTH BRUSH

K913724 is an FDA 510(k) clearance for SONEX ULTRASONIC TOOTH BRUSH, manufactured by Sonex Intl., Corp.. The device is a Class 1 Dental device with product code JEQ cleared through the Traditional 510(k) pathway after a 496-day FDA review.

K913724 · Sonex Intl., Corp. · Dental device
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Dec 1992
Decision
496d
Days
Class 1
Risk

K913724 is an FDA 510(k) clearance for the SONEX ULTRASONIC TOOTH BRUSH. Classified as Toothbrush, Powered (product code JEQ), Class I - General Controls.

Submitted by Sonex Intl., Corp. (Brewster, US). The FDA issued a Cleared decision on December 28, 1992 after a review of 496 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6865 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Dental submissions.

View all Sonex Intl., Corp. devices

FDA 510(k) Submission Details - K913724

510(k) Number K913724 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 20, 1991
Decision Date December 28, 1992
Days to Decision 496 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
369d slower than avg
Panel avg: 127d · This submission: 496d
Pathway characteristics
Predicate-based equivalence.

JEQ Device Classification - Class 1, General Controls

Product Code JEQ Toothbrush, Powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.6865
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.

Regulatory Peers - JEQ Toothbrush, Powered

All 10
Devices cleared under the same product code (JEQ) and FDA review panel - the closest regulatory comparables to K913724.
INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT
K935561 · Bausch & Lomb, Inc. · Jan 1994
OMRON RECHARGEABLE PLAQUE REMOVAL SYSTEM #HT-B142
K926246 · Omron Healthcare, Inc. · Apr 1993
OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005
K926247 · Omron Healthcare, Inc. · Apr 1993
INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT
K910610 · Bausch & Lomb, Inc. · Jul 1991