Dentsply Maillefer
FDA adverse event reports naming Dentsply Maillefer as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DENTSPLY MAILLEFER.
- Total reports
- 1,779
- Deaths
- 0
- Injuries
- 73
- Malfunctions
- 1,706
Reports per year
2308
4209
4010
13911
6212
1113
914
5915
12116
14917
14818
28619
26120
20921
822
Source: FDA adverse event reports by year received, 2008–2022. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Locator, Root ApexLQY571
- File, Pulp Canal, EndodonticEKS420
- Scaler, UltrasonicELC321
- Handpiece, Contra- And Right-Angle Attachment, DentalEGS155
- Handpiece, Direct Drive, Ac-PoweredEKX150
- Drill, Dental, IntraoralDZA50
- Post, Root CanalELR34
- Bur, DentalEJL27
- Controller, Foot, Handpiece And CordEBW21
- Plugger, Root Canal, EndodonticEKR9
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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