Cleared Traditional

K103160 - NUPRO MODEL 13016901

K103160 is an FDA 510(k) clearance for NUPRO MODEL 13016901, manufactured by CAO Group, Inc.. The device is a Class 2 Dental device with product code LBH cleared through the Traditional 510(k) pathway after a 72-day FDA review.

K103160 · CAO Group, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2011
Decision
72d
Days
Class 2
Risk

K103160 is an FDA 510(k) clearance for the NUPRO MODEL 13016901. Classified as Varnish, Cavity (product code LBH), Class II - Special Controls.

Submitted by CAO Group, Inc. (West Jordan, US). The FDA issued a Cleared decision on January 6, 2011 after a review of 72 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3260 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all CAO Group, Inc. devices

FDA 510(k) Submission Details - K103160

510(k) Number K103160 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 26, 2010
Decision Date January 06, 2011
Days to Decision 72 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
PCCP Authorized No
Regulatory Context
Review time vs. panel average
55d faster than avg
Panel avg: 127d · This submission: 72d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LBH Device Classification - Class 2, Special Controls

Product Code LBH Varnish, Cavity
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3260
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 - LBH Varnish, Cavity

All 101
Devices cleared under the same product code (LBH) and FDA review panel - the closest regulatory comparables to K103160.
PCXX VARNISH
K113146 · Ross Healthcare, Inc. · Jan 2012
ACTIV VARNISH
K112946 · Pulpdent Corporation · Dec 2011
COLGATE DESENSITIZING DENTAL CREAM
K103461 · Colgate-Palmolive Co. · Sep 2011
MI VARNISH
K102808 · GC America, Inc. · Dec 2010
TOKUYAMA SHIELD FORCE
K100172 · Tokuyama Dental Corporation · Oct 2010
ASCENT F-COAT MODEL: 006-00097
K100540 · CAO Group, Inc. · Sep 2010