Dentsply Implants Manufacturing Gmbh
FDA adverse event reports naming Dentsply Implants Manufacturing Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DENTSPLY IMPLANTS MANUFACTURING GMBH.
- Total reports
- 169,074
- Deaths
- 0
- Injuries
- 168,218
- Malfunctions
- 856
Reports per year
613
1714
2215
3416
217
2518
5,67719
1120
2321
28,55622
36,41923
38,45024
36,93625
22,89626
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Implant, Endosseous, Root-FormDZE167,792
- Abutment, Implant, Dental, EndosseousNHA752
- Accessories, Implant, Dental, EndosseousNDP515
- Bur, DentalEJL7
- Suture, DentalDZG2
- Crown And Bridge, Temporary, ResinEBG2
- File, Pulp Canal, EndodonticEKS2
- Handpiece, Rotary Bone CuttingKMW1
- System, Image Processing, RadiologicalLLZ1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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