Si-bone, Inc.
FDA adverse event reports naming Si-bone, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SI-BONE, INC..
- Total reports
- 1,158
- Deaths
- 3
- Injuries
- 1,147
- Malfunctions
- 1
Reports per year
112
4013
13714
11415
10816
14617
12918
16519
14120
14921
1622
323
424
525
Source: FDA adverse event reports by year received, 2012–2025. 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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