Cleared Traditional

K132322 - NEWTRON P5 XS B.LED

K132322 is an FDA 510(k) clearance for NEWTRON P5 XS B.LED, manufactured by Satelec - Acteon Group. The device is a Class 2 Dental device with product code ELC cleared through the Traditional 510(k) pathway after a 229-day FDA review.

K132322 · Satelec - Acteon Group · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2014
Decision
229d
Days
Class 2
Risk

K132322 is an FDA 510(k) clearance for the NEWTRON P5 XS B.LED. Classified as Scaler, Ultrasonic (product code ELC), Class II - Special Controls.

Submitted by Satelec - Acteon Group (Mt. Laurel, US). The FDA issued a Cleared decision on March 11, 2014 after a review of 229 days - an extended review 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: 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 Satelec - Acteon Group devices

FDA 510(k) Submission Details - K132322

510(k) Number K132322 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 25, 2013
Decision Date March 11, 2014
Days to Decision 229 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
102d slower than avg
Panel avg: 127d · This submission: 229d
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 79
Devices cleared under the same product code (ELC) and FDA review panel - the closest regulatory comparables to K132322.
AW-100
K171150 · Micron Corporation · Mar 2018
Cavitron Touch Ultrasonic Scaling System
K150535 · Dentsply International, Inc. · Jun 2015
EMS PIEZON 707 BIK AND PIEZON 707 BIK LED
K140990 · E.M.S Electro Medical Systems S.A · Feb 2015
PIEZON 250
K132445 · E.M.S Electro Medical Systems S.A · Dec 2013
PIEZON 150
K132443 · E.M.S Electro Medical Systems S.A · Nov 2013
R7
K130834 · Cefla S.C. · Oct 2013