Cleared Special

K030111 - DIAMONDCOAT ULTRASONIC INSERTS

K030111 is an FDA 510(k) clearance for DIAMONDCOAT ULTRASONIC INSERTS, manufactured by Dentsply International. The device is a Class 2 Dental device with product code ELC cleared through the Special 510(k) pathway after a 25-day FDA review.

K030111 · Dentsply International · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2003
Decision
25d
Days
Class 2
Risk

K030111 is an FDA 510(k) clearance for the DIAMONDCOAT ULTRASONIC INSERTS. Classified as Scaler, Ultrasonic (product code ELC), Class II - Special Controls.

Submitted by Dentsply International (York, US). The FDA issued a Cleared decision on February 7, 2003 after a review of 25 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Dentsply International devices

FDA 510(k) Submission Details - K030111

510(k) Number K030111 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 13, 2003
Decision Date February 07, 2003
Days to Decision 25 days
Submission Type Special
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
102d faster than avg
Panel avg: 127d · This submission: 25d
Pathway characteristics
Modification to existing cleared device.

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 74
Devices cleared under the same product code (ELC) and FDA review panel - the closest regulatory comparables to K030111.
SIROSON L AND SIROSONIC L ULTRASONIC SCALERS
K033640 · Sirona Dental Systems GmbH · Dec 2003
BOBCAT PRO SCALER SYSTEM, MODEL G-130
K033705 · Dentsply International · Dec 2003
CARRIER TIPS
K031461 · Dentsply Intl. · Aug 2003
STERI-MATE STERILIZABLE HANDPIECE
K023697 · Dentsply International · Nov 2002
PREMIER ULTRASONIC SCALER AND INSERTS
K010195 · Premier Dental Products Co. · Apr 2001
SP4044 & SP4055 LUX MODULES
K972026 · Satelec · Jul 1997