Cleared Traditional

K053178 - SYMMETRY S-SERIES PIEZOELECTRIC SCALING TIPS

K053178 is an FDA 510(k) clearance for SYMMETRY S-SERIES PIEZOELECTRIC SCALING..., manufactured by Hu-Friedy Mfg. Co., Inc.. The device is a Class 2 Dental device with product code ELC cleared through the Traditional 510(k) pathway after a 79-day FDA review.

K053178 · Hu-Friedy Mfg. Co., Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2006
Decision
79d
Days
Class 2
Risk

K053178 is an FDA 510(k) clearance for the SYMMETRY S-SERIES PIEZOELECTRIC SCALING TIPS. Classified as Scaler, Ultrasonic (product code ELC), Class II - Special Controls.

Submitted by Hu-Friedy Mfg. Co., Inc. (Chicago, US). The FDA issued a Cleared decision on February 1, 2006 after a review of 79 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4850 - 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 Hu-Friedy Mfg. Co., Inc. devices

FDA 510(k) Submission Details - K053178

510(k) Number K053178 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 14, 2005
Decision Date February 01, 2006
Days to Decision 79 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
48d faster than avg
Panel avg: 127d · This submission: 79d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ELC Device Classification - Class 2, Special Controls

Product Code ELC Scaler, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.4850
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Dental devices follow this clearance model.

Regulatory Peers - ELC Scaler, Ultrasonic

All 84
Devices cleared under the same product code (ELC) and FDA review panel - the closest regulatory comparables to K053178.
ULTRASONIC SCALER, VARIOS 560
K062731 · Nakanishi, Inc. · May 2007
ASC-12 PIEZOELECTRIC SCALER
K070866 · Aseptico, Inc. · Apr 2007
PIEZOTOME
K060275 · Satelec · May 2006
J. MORITA AZ ULTRASONIC SYSTEM
K053030 · J. Morita USA, Inc. · Nov 2005
CAVITRON RF ULTRASONIC SCALER SYSTEM WITH STERIMATE HANDPIECE, MODEL G-131
K052334 · Dentsply Intl. · Sep 2005
SURPASSON P5 NEWTRON
K050895 · Satelec · Apr 2005