Dentsply LLC
FDA adverse event reports naming Dentsply LLC as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DENTSPLY LLC.
- Total reports
- 1,925
- Deaths
- 1
- Injuries
- 68
- Malfunctions
- 1,856
Reports per year
12918
22019
9920
9921
11622
21123
23724
28825
52626
Source: FDA adverse event reports by year received, 2018–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Scaler, UltrasonicELC1,299
- Instruments, Dental HandDZN266
- Unit, X-Ray, IntraoralEAP259
- Mask, SurgicalFXX30
- Agent, Polishing, Abrasive, Oral CavityEJR16
- Activator, Ultraviolet, For PolymerizationEBZ10
- Material, ImpressionELW10
- Cement, DentalEMA7
- Resin, Denture, Relining, Repairing, RebasingEBI5
- Orthodontic Vibratory AccessoryOYH5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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