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Straumann Dental Implant System Roxolid SLA Impl.Recalls & reported problems across all models

Institut Straumann AG · 80 models in the FDA device registry

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
377,342
Deaths reported
0
Injuries reported
377,342
Recalls
0

We found 80 models of Straumann Dental Implant System Roxolid SLA Impl. by Institut Straumann AG in the FDA's device registry (GUDID). Together they are named in 377,342 adverse event reports in the FDA's MAUDE database, received between Apr 30, 2018 and Sep 30, 2026 — classified as 377,342 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (254,484 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: 4,496 reportsDec 2023: 4,643 reportsJan 2024: 4,173 reportsFeb 2024: 4,549 reportsMar 2024: 4,505 reportsApr 2024: 5,944 reportsMay 2024: 4,643 reportsJun 2024: 4,729 reportsJul 2024: 4,944 reportsAug 2024: 4,607 reportsSep 2024: 4,909 reportsOct 2024: 7,814 reportsNov 2024: 7,269 reportsDec 2024: 4,383 reportsJan 2025: 5,134 reportsFeb 2025: 4,139 reportsMar 2025: 5,317 reportsApr 2025: 1,786 reportsMay 2025: 1 reportsJun 2025: 14,671 reportsJul 2025: 5,703 reportsAug 2025: 5,565 reportsSep 2025: 3,481 reportsOct 2025: 4,630 reportsNov 2025: 5,461 reportsDec 2025: 6,287 reportsJan 2026: 5,122 reportsFeb 2026: 4,778 reportsMar 2026: 5,982 reportsApr 2026: 5,959 reportsMay 2026: 5,955 reportsJun 2026: 4,895 reportsJul 2026: 4,867 reportsAug 2026: 3,686 reportsSep 2026: 3,100 reportsOct 2026: 0 reports20242025202614,671
Last 36 months. The most recent month may be incomplete.

Most reported Straumann Dental Implant System Roxolid SLA Impl. problems

Device problems

  • Failure to Osseointegrate254,484
  • Loss of Osseointegration100,748
  • Adverse Event Without Identified Device or Use Problem15,790
  • Fracture4,696
  • Difficult to Insert2,457
  • Separation Failure517
  • Unintended Movement327
  • Unstable225

Patient problems

  • No Clinical Signs, Symptoms or Conditions142,835
  • Fibrosis129,875
  • Pain84,358
  • Unspecified Infection62,640
  • Tissue Damage38,306
  • Inflammation26,851
  • Hemorrhage/Blood Loss/Bleeding21,340
  • Swelling/ Edema19,686

Straumann Dental Implant System Roxolid SLA Impl. models

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

Recent Straumann Dental Implant System Roxolid SLA Impl. 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