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
- 1,167,338
- Deaths
- 1
- Injuries
- 1,167,327
- Malfunctions
- 2
Reports per year
104
105
107
3111
812
114
74718
71,33719
95,06420
110,56921
149,06222
178,59923
212,02624
233,76125
115,73026
Source: FDA adverse event reports by year received, 2004–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Implant, Endosseous, Root-FormDZE1,166,958
- Implant, Endosseous, OrthodonticOAT322
- 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.
Monitor Institut Straumann Ag automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.