Implant Direct Sybron Manufact
FDA adverse event reports naming Implant Direct Sybron Manufact as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: IMPLANT DIRECT SYBRON MANUFACT.
- Total reports
- 12,184
- Deaths
- 3
- Injuries
- 12,092
- Malfunctions
- 89
Reports per year
46323
4,75724
4,56325
2,40126
Source: FDA adverse event reports by year received, 2023–2026. 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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