Cleared Special

K111814 - PADLOCK

K111814 is an FDA 510(k) clearance for PADLOCK, manufactured by Reliance Orthodontic Products, Inc.. The device is a Class 2 Dental device with product code DYH cleared through the Special 510(k) pathway after a 79-day FDA review.

K111814 · Reliance Orthodontic Products, Inc. · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Sep 2011
Decision
79d
Days
Class 2
Risk

K111814 is an FDA 510(k) clearance for the PADLOCK. Classified as Adhesive, Bracket And Tooth Conditioner, Resin (product code DYH), Class II - Special Controls.

Submitted by Reliance Orthodontic Products, Inc. (Itasca, US). The FDA issued a Cleared decision on September 14, 2011 after a review of 79 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3750 - 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.

FDA 510(k) Submission Details - K111814

510(k) Number K111814 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 27, 2011
Decision Date September 14, 2011
Days to Decision 79 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
49d faster than avg
Panel avg: 128d · This submission: 79d
Pathway characteristics
Modification to existing cleared device.

DYH Device Classification - Class 2, Special Controls

Product Code DYH Adhesive, Bracket And Tooth Conditioner, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3750
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 - DYH Adhesive, Bracket And Tooth Conditioner, Resin

All 193
Devices cleared under the same product code (DYH) and FDA review panel - the closest regulatory comparables to K111814.
ORTHODONTIC FLOWABLE BRACKET ADHESIVE
K120619 · Novocol, Inc. · May 2012
ORTHO-1(NOT FINALIZED)
K113401 · Bisco, Inc. · Feb 2012
APC FLASH-FREE ADHESIVE
K113197 · 3M Unitek Corporation · Feb 2012
OPAL BAND CEMENT
K111696 · Ultradent Products, Inc. · Sep 2011
LIGHT CURE RETAINER
K101951 · Reliance Orthodontic Products, Inc. · Oct 2010
TRANSBOND IDB PRE-MIX CHEMICAL CARE ADHESIVE
K100536 · 3M Unitek · Jul 2010
K111814 · PADLOCK
Download PDF FDA Summary Reliance Orthodontic …