Cleared Traditional

ROTA-DENT TOOTH CLEANER (K880589) - FDA 510(k) Clearance

Class I Dental device.

K880589 · Pro-Dentec · Dental device
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May 1988
Decision
90d
Days
Class 1
Risk

K880589 is an FDA 510(k) clearance for the ROTA-DENT TOOTH CLEANER. Classified as Toothbrush, Powered (product code JEQ), Class I - General Controls.

Submitted by Pro-Dentec (Chicago, US). The FDA issued a Cleared decision on May 11, 1988 after a review of 90 days - within the typical 510(k) review window.

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: 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 Pro-Dentec devices

Submission Details

510(k) Number K880589 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 11, 1988
Decision Date May 11, 1988
Days to Decision 90 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
37d faster than avg
Panel avg: 127d · This submission: 90d
Pathway characteristics
Predicate-based equivalence.

Device Classification

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.