Dentsply Tulsa
FDA adverse event reports naming Dentsply Tulsa as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DENTSPLY TULSA.
- Total reports
- 1,382
- Deaths
- 0
- Injuries
- 139
- Malfunctions
- 1,239
Reports per year
10703
21104
38105
38406
12007
9308
8509
113
Source: FDA adverse event reports by year received, 2003–2013. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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