Bonart Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K162856Bonart Dental Handpieces (ART), Disposable Prophy Angle (PROFORMANCE)July 18, 2017
K152125Oral Surgery System and AccessoriesAugust 15, 2016
K100785BONART MODEL ART-IM1 IMPLANTOR SYSTEM & ACCESSORIESDecember 3, 2010
K082971BONART ART-L5 LED CORDLESS CURING LIGHTNovember 13, 2008
K081550BONART ULTRASONIC SCALER, MOEDLS ART-P3II PRO AND ART-MII PROAugust 28, 2008
K080761BONART'S ARTEOTOMY OMI AND OPI ULTRASONIC SURGERY SYSTEM & ACCESSORIESAugust 25, 2008
K071981BONART MODEL ART-P6 PIEZO ELECTRIC ULTRASONIC SCALER & ACCESSORIES (TIPS)October 26, 2007
K062289BONART ART-L3 LED CURING LIGHTJanuary 3, 2007
K061448BONART ART-P3II & P4 PIEZO ELECTRIC ULTRASONIC SCALER UNITS WITH ACCESSORIESAugust 17, 2006
K052028BONART ART-M3II & M4 ULTRASONIC SCALER UNITS WITH ACCESSORIES (INSERTS)October 28, 2005
K023721BONART ART-L2 LIGHT CURING UNITJanuary 10, 2003
K000510ART-M1, MODEL M1-1-ART-A1May 15, 2000
K994299ART-P3, MODEL P3-1-ART-A1March 6, 2000
K994203ART-M3 25K, MODEL M3-1-ART2-A1; ART-M3 30K, MODEL M3-1-ART3-A1March 6, 2000