Bonart Co., Ltd.
Bonart Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2017.
Top product codes for Bonart Co., Ltd.
Recent clearances by Bonart Co., Ltd.
- K162856 — Bonart Dental Handpieces (ART), Disposable Prophy Angle (PROFORMANCE)
- K152125 — Oral Surgery System and Accessories
- K100785 — BONART MODEL ART-IM1 IMPLANTOR SYSTEM & ACCESSORIES
- K082971 — BONART ART-L5 LED CORDLESS CURING LIGHT
- K081550 — BONART ULTRASONIC SCALER, MOEDLS ART-P3II PRO AND ART-MII PRO
- K080761 — BONART'S ARTEOTOMY OMI AND OPI ULTRASONIC SURGERY SYSTEM & ACCESSORIES
- K071981 — BONART MODEL ART-P6 PIEZO ELECTRIC ULTRASONIC SCALER & ACCESSORIES (TIPS)
- K062289 — BONART ART-L3 LED CURING LIGHT
- K061448 — BONART ART-P3II & P4 PIEZO ELECTRIC ULTRASONIC SCALER UNITS WITH ACCESSORIES
- K052028 — BONART ART-M3II & M4 ULTRASONIC SCALER UNITS WITH ACCESSORIES (INSERTS)
- K023721 — BONART ART-L2 LIGHT CURING UNIT
- K000510 — ART-M1, MODEL M1-1-ART-A1
- K994203 — ART-M3 25K, MODEL M3-1-ART2-A1; ART-M3 30K, MODEL M3-1-ART3-A1
- K994299 — ART-P3, MODEL P3-1-ART-A1
Data sourced from openFDA. This site is unofficial and independent of the FDA.