Dentium USA
FDA adverse event reports naming Dentium USA as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DENTIUM USA.
- Total reports
- 1,567
- Deaths
- 0
- Injuries
- 1,550
- Malfunctions
- 0
Reports per year
9011
412
913
1614
2215
1316
13817
13618
13220
18221
12022
14723
16524
15825
7226
Source: FDA adverse event reports by year received, 2011–2026. 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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