Cleared Abbreviated

K060744 - O'BRIEN MPA (MANDIBULAR POSITIONING APPLICANCE)

K060744 is an FDA 510(k) clearance for O'BRIEN MPA (MANDIBULAR POSITIONING APP..., manufactured by O'Brien Dental Lab, Inc.. The device is a Class 2 Dental device with product code LRK cleared through the Abbreviated 510(k) pathway after a 74-day FDA review.

K060744 · O'Brien Dental Lab, Inc. · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Jun 2006
Decision
74d
Days
Class 2
Risk

K060744 is an FDA 510(k) clearance for the O'BRIEN MPA (MANDIBULAR POSITIONING APPLICANCE). Classified as Device, Anti-snoring (product code LRK), Class II - Special Controls.

Submitted by O'Brien Dental Lab, Inc. (Corvallis, US). The FDA issued a Cleared decision on June 2, 2006 after a review of 74 days - a notably fast clearance 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 - K060744

510(k) Number K060744 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 20, 2006
Decision Date June 02, 2006
Days to Decision 74 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
54d faster than avg
Panel avg: 128d · This submission: 74d
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 216
Devices cleared under the same product code (LRK) and FDA review panel - the closest regulatory comparables to K060744.
TAP III ANTI-SNORING DEVICE
K062951 · Airway Management, Inc. · Dec 2006
ANTI-SNORING / SLEEP APNEA DEVICE
K061688 · Tomed Dr. Toussaint GmbH · Sep 2006
TAP-T
K061732 · Airway Management, Inc. · Jul 2006
SLEEP SPLINT
K060122 · Nakagawa Dental Clinic · May 2006
TAP II ANTI-SNORING AND OBSTRUCTIVE SLEEP APNEA ORAL APPLIANCE WITH ATTACHMENT
K060388 · Airway Management, Inc. · May 2006
SILENT PARTNER SERIES OSA APPLIANCES
K051014 · Dreamwrx Dental Laboratory · Aug 2005
K060744 · O'BRIEN MPA (MANDIBULAR POSITIONING APPLICANCE)
Download PDF FDA Summary O'Brien Dental Lab, I…