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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.
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