Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

CAO Group, Inc. — Predicate Candidate Screening

31 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

137 daysmedian FDA review time
297 days90th percentile
31clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K254197Picasso Pro Diode Laser (002-00460)CAO Group, Inc.2026-03-11780
K201904Monet Curing LaserCAO Group, Inc.2020-11-241380
K201475Ultimate Contour, Ultimate Contour MiniCAO Group, Inc.2020-10-281470
K181614Sterling Supreme Diode LaserCAO Group, Inc.2019-09-104480
K181602Pioneer Elite Diode LaserCAO Group, Inc.2019-09-104480
K181601Precise SHP Diode LaserCAO Group, Inc.2019-09-094470
K171052Ultimate Contour, Ultimate Contour MiniCAO Group, Inc.2017-10-201930
K171986Sterling Supreme Diode LaserCAO Group, Inc.2017-09-22810
K160413Sterling 5W Diode LaserCAO Group, Inc.2016-09-212180
K150585Ascent 3DCAO Group, Inc.2015-12-312970
K142226Pilot Ultra Diode LaserCAO Group, Inc.2014-09-12300
K142223Pilot Pro Diode LaserCAO Group, Inc.2014-09-12300
K142225Pilot Elite Diode LaserCAO Group, Inc.2014-09-12300
K131059PIONEER ELITE DIODE LASERCAO Group, Inc.2013-09-131500
K123443PRECISE SHP DIODE LASERCAO Group, Inc.2013-08-132780
K113472PRECISE SHP DIODE LASERCAO Group, Inc.2012-08-302820
K103160NUPRO MODEL 13016901CAO Group, Inc.2011-01-06720
K100540ASCENT F-COAT MODEL: 006-00097CAO Group, Inc.2010-09-232100
K100143PILOT DIODE LASER, MODEL 002-00139CAO Group, Inc.2010-08-132060
K092616ASCENT BOND UNIVERSAL ADHESIVE SYSTEM, MODELS 006-00029, 006CAO Group, Inc.2009-10-21560
K091300ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079CAO Group, Inc.2009-07-23800
K070070ASCENT DENTAL CLEANSERCAO Group, Inc.2007-05-251370
K070413ASCENT UNIVERSAL ADHESIVE, MODEL 006-00028CAO Group, Inc.2007-04-26730
K062619DENLASER 800 PLUSCAO Group, Inc.2006-11-14700
K062886ASCENT PIT AND FISSURE SEALANT, MODEL 006-00019CAO Group, Inc.2006-11-06410
K061366DENLASER 800 PLUSCAO Group, Inc.2006-07-10550
K061341PALMLIGHT 10, MODEL 001-00030CAO Group, Inc.2006-06-12280
K053089ASCENT PIT & FISSURE SEALANTCAO Group, Inc.2005-12-20480
K041392SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, CAO Group, Inc.2004-11-081670
K020057PALMLIGHTCAO Group, Inc.2002-08-272310
K003541DENLASER, MODEL 800CAO Group, Inc.2001-01-257012

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda