Cleared Abbreviated

K082849 - SILENT SLEEP

K082849 is an FDA 510(k) clearance for SILENT SLEEP, manufactured by Craniofacial Pain Center of Idaho. The device is a Class 2 Dental device with product code LRK cleared through the Abbreviated 510(k) pathway after a 290-day FDA review.

K082849 · Craniofacial Pain Center of Idaho · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2009
Decision
290d
Days
Class 2
Risk

K082849 is an FDA 510(k) clearance for the SILENT SLEEP. Classified as Device, Anti-snoring (product code LRK), Class II - Special Controls.

Submitted by Craniofacial Pain Center of Idaho (Boise, US). The FDA issued a Cleared decision on July 16, 2009 after a review of 290 days - an extended review cycle.

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.

FDA 510(k) Submission Details - K082849

510(k) Number K082849 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2008
Decision Date July 16, 2009
Days to Decision 290 days
Submission Type Abbreviated
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
162d slower than avg
Panel avg: 128d · This submission: 290d
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 214
Devices cleared under the same product code (LRK) and FDA review panel - the closest regulatory comparables to K082849.
THE MOSES APPLIANCE
K093710 · Allen J. Moses, Dds, Ltd. · May 2010
AIRWAYEASE MAS
K090436 · Orthoplant Dental Lab · Apr 2010
VITAL SLEEP
K092942 · The Snore Reliever Company, LLC · Jan 2010
ZQUIET MOUTHPIECE
K090503 · Sleeping Well, LLC · Mar 2009
ACRYLIC HERBST SPLINT APPLIANCE
K083209 · Specialty Appliance Works, Inc. · Jan 2009
MPOWRX SNORING SOLUTION
K081965 · Mpowrx Health and Wellness Products, Inc. · Oct 2008
K082849 · SILENT SLEEP
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