Cleared Abbreviated

K171529 - Snorer's Friend

K171529 is an FDA 510(k) clearance for Snorer's Friend, manufactured by Scope Healthcare Technologies Pty, Ltd.. The device is a Class 2 Dental device with product code LRK cleared through the Abbreviated 510(k) pathway after a 222-day FDA review.

K171529 · Scope Healthcare Technologies Pty, Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2018
Decision
222d
Days
Class 2
Risk

K171529 is an FDA 510(k) clearance for the Snorer's Friend. Classified as Device, Anti-snoring (product code LRK), Class II - Special Controls.

Submitted by Scope Healthcare Technologies Pty, Ltd. (Unley, AU). The FDA issued a Cleared decision on January 2, 2018 after a review of 222 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.

View all Scope Healthcare Technologies Pty, Ltd. devices

FDA 510(k) Submission Details - K171529

510(k) Number K171529 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 25, 2017
Decision Date January 02, 2018
Days to Decision 222 days
Submission Type Abbreviated
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
95d slower than avg
Panel avg: 127d · This submission: 222d
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 85
Devices cleared under the same product code (LRK) and FDA review panel - the closest regulatory comparables to K171529.
ZQuiet
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The Panthera Anti-Snoring X3 Device
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MEDTRONIC XOMED, INC.
K122391 · Medtronic Xomed, Inc. · Jan 2013
PILLAR PALATAL IMPLANT SYSTEM
K110623 · Medtronic Xomed, Inc. · Feb 2012
REMOVABLE ARYLIC HERBST, ALLESEE SNORE APPLIANCE (ASA), AND ENOCH SNORINATOR
K070327 · Sybron Dental Specialties, Inc. · May 2007