Skip to content

Straumann BLC and TLC ImplantsRecalls & reported problems across all models

Institut Straumann AG · 153 models in the FDA device registry

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

Adverse event reports
20,568
Deaths reported
0
Injuries reported
20,568
Recalls
0

We found 153 models of Straumann BLC and TLC Implants by Institut Straumann AG in the FDA's device registry (GUDID). Together they are named in 20,568 adverse event reports in the FDA's MAUDE database, received between Feb 9, 2024 and Sep 28, 2026 — classified as 20,568 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (15,068 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: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 6 reportsMar 2024: 3 reportsApr 2024: 24 reportsMay 2024: 29 reportsJun 2024: 93 reportsJul 2024: 115 reportsAug 2024: 141 reportsSep 2024: 243 reportsOct 2024: 241 reportsNov 2024: 357 reportsDec 2024: 200 reportsJan 2025: 409 reportsFeb 2025: 286 reportsMar 2025: 451 reportsApr 2025: 149 reportsMay 2025: 0 reportsJun 2025: 1,589 reportsJul 2025: 789 reportsAug 2025: 808 reportsSep 2025: 430 reportsOct 2025: 767 reportsNov 2025: 928 reportsDec 2025: 1,155 reportsJan 2026: 980 reportsFeb 2026: 1,118 reportsMar 2026: 1,492 reportsApr 2026: 1,395 reportsMay 2026: 1,486 reportsJun 2026: 1,241 reportsJul 2026: 1,387 reportsAug 2026: 1,283 reportsSep 2026: 973 reportsOct 2026: 0 reports2024202520261,589
Last 36 months. The most recent month may be incomplete.

Most reported Straumann BLC and TLC Implants problems

Device problems

  • Failure to Osseointegrate15,068
  • Adverse Event Without Identified Device or Use Problem2,999
  • Loss of Osseointegration1,940
  • Difficult to Insert493
  • Separation Failure93
  • Fracture27

Patient problems

  • No Clinical Signs, Symptoms or Conditions11,004
  • Fibrosis6,872
  • Pain3,545
  • Unspecified Infection2,476
  • Inflammation1,108
  • Swelling/ Edema802
  • Hemorrhage/Blood Loss/Bleeding730
  • Hyperresponsive to stimuli541

Straumann BLC and TLC Implants models

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

Recent Straumann BLC and TLC Implants 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