Atlas FDA

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

Bonart Co., Ltd. · Predicate Candidate Screening

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

93 daysmedian FDA review time
279 days90th percentile
14clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K162856Bonart Dental Handpieces (ART), Disposable Prophy Angle (PROBonart Co., Ltd.2017-07-182790
K152125Oral Surgery System and AccessoriesBonart Co., Ltd.2016-08-153810
K100785BONART MODEL ART-IM1 IMPLANTOR SYSTEM & ACCESSORIESBonart Co., Ltd.2010-12-032590
K082971BONART ART-L5 LED CORDLESS CURING LIGHTBonart Co., Ltd.2008-11-13380
K081550BONART ULTRASONIC SCALER, MOEDLS ART-P3II PRO AND ART-MII PRBonart Co., Ltd.2008-08-28860
K080761BONART'S ARTEOTOMY OMI AND OPI ULTRASONIC SURGERY SYSTEM & ABonart Co., Ltd.2008-08-251600
K071981BONART MODEL ART-P6 PIEZO ELECTRIC ULTRASONIC SCALER & ACCESBonart Co., Ltd.2007-10-261000
K062289BONART ART-L3 LED CURING LIGHTBonart Co., Ltd.2007-01-031490
K061448BONART ART-P3II & P4 PIEZO ELECTRIC ULTRASONIC SCALER UNITS Bonart Co., Ltd.2006-08-17870
K052028BONART ART-M3II & M4 ULTRASONIC SCALER UNITS WITH ACCESSORIEBonart Co., Ltd.2005-10-28930
K023721BONART ART-L2 LIGHT CURING UNITBonart Co., Ltd.2003-01-10660
K000510ART-M1, MODEL M1-1-ART-A1Bonart Co., Ltd.2000-05-15900
K994203ART-M3 25K, MODEL M3-1-ART2-A1; ART-M3 30K, MODEL M3-1-ART3-Bonart Co., Ltd.2000-03-06840
K994299ART-P3, MODEL P3-1-ART-A1Bonart Co., Ltd.2000-03-06760

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