Institut Straumann Ag
FDA adverse event reports naming Institut Straumann Ag as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: INSTITUT STRAUMANN AG.
- Total reports
- 1,180,015
- Deaths
- 1
- Injuries
- 1,180,004
- Malfunctions
- 2
Reports per year
104
105
107
3111
812
114
74718
71,33719
95,06420
110,56921
149,06222
178,59823
212,02624
233,74825
128,42126
Source: FDA adverse event reports by year received, 2004–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Implant, Endosseous, Root-FormDZE1,179,634
- Implant, Endosseous, OrthodonticOAT323
- Barrier, Synthetic, IntraoralNPK24
- Bone Grafting Material, SyntheticLYC12
- Abutment, Implant, Dental, EndosseousNHA6
- Accessories, Implant, Dental, EndosseousNDP5
- Prosthesis, Breast, External, Used With AdhesiveKCZ4
- Biologic Material, DentalNQA2
- Drill, Dental, IntraoralDZA1
- Handle, Instrument, DentalEJB1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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