FDA 510(k) Applications Submitted by BONART CO. LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K000510 02/15/2000 ART-M1, MODEL M1-1-ART-A1 BONART CO. LTD.
K994203 12/13/1999 ART-M3 25K, MODEL M3-1-ART2-A1; ART-M3 30K, MODEL M3-1-ART3-A1 BONART CO. LTD.
K994299 12/21/1999 ART-P3, MODEL P3-1-ART-A1 BONART CO. LTD.
K080761 03/18/2008 BONART'S ARTEOTOMY OMI AND OPI ULTRASONIC SURGERY SYSTEM & ACCESSORIES BONART CO. LTD.
K100785 03/19/2010 BONART MODEL ART-IM1 IMPLANTOR SYSTEM & ACCESSORIES BONART CO. LTD.
K061448 05/22/2006 BONART ART-P3II & P4 PIEZO ELECTRIC ULTRASONIC SCALER UNITS WITH ACCESSORIES BONART CO. LTD.
K081550 06/03/2008 BONART ULTRASONIC SCALER, MOEDLS ART-P3II PRO AND ART-MII PRO BONART CO. LTD.
K071981 07/18/2007 BONART MODEL ART-P6 PIEZO ELECTRIC ULTRASONIC SCALER & ACCESSORIES (TIPS) BONART CO. LTD.
K052028 07/27/2005 BONART ART-M3II & M4 ULTRASONIC SCALER UNITS WITH ACCESSORIES (INSERTS) BONART CO. LTD.
K062289 08/07/2006 BONART ART-L3 LED CURING LIGHT BONART CO. LTD.
K082971 10/06/2008 BONART ART-L5 LED CORDLESS CURING LIGHT BONART CO. LTD.
K023721 11/05/2002 BONART ART-L2 LIGHT CURING UNIT BONART CO. LTD.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact