Cleared Traditional

K923711 - PERIOFLEX TIP

K923711 is an FDA 510(k) clearance for PERIOFLEX TIP, manufactured by Novadent, Ltd.. The device is a Class 1 Dental device with product code EFS cleared through the Traditional 510(k) pathway after a 658-day FDA review.

K923711 · Novadent, Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1994
Decision
658d
Days
Class 1
Risk

K923711 is an FDA 510(k) clearance for the PERIOFLEX TIP. Classified as Unit, Oral Irrigation (product code EFS), Class I - General Controls.

Submitted by Novadent, Ltd. (Jerusalem, IL). The FDA issued a Cleared decision on May 16, 1994 after a review of 658 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6510 - 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 Novadent, Ltd. devices

FDA 510(k) Submission Details - K923711

510(k) Number K923711 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 27, 1992
Decision Date May 16, 1994
Days to Decision 658 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
531d slower than avg
Panel avg: 127d · This submission: 658d
Pathway characteristics
Predicate-based equivalence.

EFS Device Classification - Class 1, General Controls

Product Code EFS Unit, Oral Irrigation
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.6510
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 - EFS Unit, Oral Irrigation

All 8
Devices cleared under the same product code (EFS) and FDA review panel - the closest regulatory comparables to K923711.
AGATHA-A-H2010
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MAX-I-PROBE IRRIGATION SYSTEM
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ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES
K900178 · Core-Vent Corp. · May 1990
PERIODONTAL SCALING SOLUTION-A
K875132 · Dentsply Intl. · Feb 1988