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STRAUMANN DENTAL IMPLANT SYSTEMRecalls & reported problems across all models

Institut Straumann AG · 128 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
98,339
Deaths reported
0
Injuries reported
98,339
Recalls
0

We found 128 models of STRAUMANN DENTAL IMPLANT SYSTEM by Institut Straumann AG in the FDA's device registry (GUDID). Together they are named in 98,339 adverse event reports in the FDA's MAUDE database, received between Oct 31, 2018 and Sep 28, 2026 — classified as 98,339 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (62,692 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Reports received per month, all models

Nov 2023: 1,714 reportsDec 2023: 1,584 reportsJan 2024: 1,480 reportsFeb 2024: 1,377 reportsMar 2024: 1,182 reportsApr 2024: 1,860 reportsMay 2024: 1,207 reportsJun 2024: 1,417 reportsJul 2024: 1,312 reportsAug 2024: 906 reportsSep 2024: 1,518 reportsOct 2024: 1,084 reportsNov 2024: 1,317 reportsDec 2024: 847 reportsJan 2025: 1,070 reportsFeb 2025: 724 reportsMar 2025: 1,127 reportsApr 2025: 345 reportsMay 2025: 0 reportsJun 2025: 3,426 reportsJul 2025: 969 reportsAug 2025: 1,218 reportsSep 2025: 633 reportsOct 2025: 646 reportsNov 2025: 1,040 reportsDec 2025: 1,215 reportsJan 2026: 1,011 reportsFeb 2026: 807 reportsMar 2026: 844 reportsApr 2026: 871 reportsMay 2026: 724 reportsJun 2026: 714 reportsJul 2026: 898 reportsAug 2026: 579 reportsSep 2026: 458 reportsOct 2026: 0 reports2024202520263,426
Last 36 months. The most recent month may be incomplete.

Most reported STRAUMANN DENTAL IMPLANT SYSTEM problems

Device problems

  • Failure to Osseointegrate62,692
  • Loss of Osseointegration30,616
  • Fracture3,680
  • Adverse Event Without Identified Device or Use Problem1,754
  • Difficult to Insert271
  • Unintended Movement89
  • Unstable77
  • Separation Failure44

Patient problems

  • No Clinical Signs, Symptoms or Conditions49,269
  • Fibrosis20,740
  • Unspecified Infection14,822
  • Pain14,550
  • Tissue Damage12,298
  • Inflammation7,700
  • Hemorrhage/Blood Loss/Bleeding6,370
  • Swelling/ Edema4,850

STRAUMANN DENTAL IMPLANT SYSTEM models

128 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.

Recent STRAUMANN DENTAL IMPLANT SYSTEM adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Institut Straumann AG products

All Institut Straumann AG devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page