Dentsply VDW Gmbh
FDA adverse event reports naming Dentsply VDW Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DENTSPLY VDW GMBH.
- Total reports
- 1,640
- Deaths
- 0
- Injuries
- 47
- Malfunctions
- 1,592
Reports per year
806
707
110
511
112
813
214
3815
6516
11517
25318
49719
32120
28921
222
Source: FDA adverse event reports by year received, 2006–2022. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- File, Pulp Canal, EndodonticEKS555
- Locator, Root ApexLQY489
- Syringe, Periodontic, Endodontic, IrrigatingEIC260
- Handpiece, Contra- And Right-Angle Attachment, DentalEGS192
- Controller, Foot, Handpiece And CordEBW101
- Reamer, Pulp Canal, EndodonticEKP14
- Instrument, Filling, Plastic, DentalEIY11
- Gutta-PerchaEKM5
- Plugger, Root Canal, EndodonticEKR4
- Drill, Dental, IntraoralDZA3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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