Cleared Abbreviated

K051014 - SILENT PARTNER SERIES OSA APPLIANCES

K051014 is an FDA 510(k) clearance for SILENT PARTNER SERIES OSA APPLIANCES, manufactured by Dreamwrx Dental Laboratory. The device is a Class 2 Dental device with product code LRK cleared through the Abbreviated 510(k) pathway after a 110-day FDA review.

K051014 · Dreamwrx Dental Laboratory · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2005
Decision
110d
Days
Class 2
Risk

K051014 is an FDA 510(k) clearance for the SILENT PARTNER SERIES OSA APPLIANCES. Classified as Device, Anti-snoring (product code LRK), Class II - Special Controls.

Submitted by Dreamwrx Dental Laboratory (Los Angeles, US). The FDA issued a Cleared decision on August 9, 2005 after a review of 110 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.5570 - the FDA dental device regulatory framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Dreamwrx Dental Laboratory devices

FDA 510(k) Submission Details - K051014

510(k) Number K051014 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 21, 2005
Decision Date August 09, 2005
Days to Decision 110 days
Submission Type Abbreviated
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
17d faster than avg
Panel avg: 127d · This submission: 110d
Pathway characteristics
Standards-based clearance path.

LRK Device Classification - Class 2, Special Controls

Product Code LRK Device, Anti-snoring
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.5570
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 - LRK Device, Anti-snoring

All 125
Devices cleared under the same product code (LRK) and FDA review panel - the closest regulatory comparables to K051014.
ACRYLIC HERBST APPLIANCE
K111009 · Embassy Dental Laboratory · Jul 2011
APNEA GUARD
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REMOVABLE ARYLIC HERBST, ALLESEE SNORE APPLIANCE (ASA), AND ENOCH SNORINATOR
K070327 · Sybron Dental Specialties, Inc. · May 2007
RESPIRONICS CUSTOM I ORAL APPLIANCE
K033822 · Respironics, Inc. · Feb 2004
RESPIRONICS CUSTOM II ORAL APPLIANCE
K033823 · Respironics, Inc. · Feb 2004
TONGUE STABILIZER DEVICE
K993381 · University of Otago · Dec 1999