Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Bonart Co., Ltd. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jul 18, 2017: Bonart Dental Handpieces (ART), Disposable Prophy Angle (PROFORMANCE).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jul 18, 2017 | Bonart Dental Handpieces (ART), Disposable Prophy Angle (PROFORMANCE)K162856 · EGS | 510(k) clearances |
| Aug 15, 2016 | Oral Surgery System and AccessoriesK152125 · DZI | 510(k) clearances |
| Dec 3, 2010 | BONART MODEL ART-IM1 IMPLANTOR SYSTEM & ACCESSORIESK100785 · EBW | 510(k) clearances |
| Nov 13, 2008 | BONART ART-L5 LED CORDLESS CURING LIGHTK082971 · EBZ | 510(k) clearances |
| Aug 28, 2008 | BONART ULTRASONIC SCALER, MOEDLS ART-P3II PRO AND ART-MII PROK081550 · ELC | 510(k) clearances |
| Aug 25, 2008 | BONART'S ARTEOTOMY OMI AND OPI ULTRASONIC SURGERY SYSTEM & ACCESSORIESK080761 · DZI | 510(k) clearances |
| Oct 26, 2007 | BONART MODEL ART-P6 PIEZO ELECTRIC ULTRASONIC SCALER & ACCESSORIES (TIPS)K071981 · ELC | 510(k) clearances |
| Jan 3, 2007 | BONART ART-L3 LED CURING LIGHTK062289 · EBZ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
