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NobelActiveRecalls & reported problems across all models

Nobel Biocare AB · 56 models in the FDA device registry

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

Adverse event reports
152,066
Deaths reported
2
Injuries reported
150,407
Recalls
0

We found 56 models of NobelActive by Nobel Biocare AB in the FDA's device registry (GUDID). Together they are named in 152,066 adverse event reports in the FDA's MAUDE database, received between Oct 11, 2017 and Sep 30, 2026 — classified as 2 deaths, 150,407 injuries, 1,657 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (83,253 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: 2,365 reportsDec 2023: 1,914 reportsJan 2024: 2,532 reportsFeb 2024: 1,912 reportsMar 2024: 2,346 reportsApr 2024: 2,365 reportsMay 2024: 2,035 reportsJun 2024: 1,909 reportsJul 2024: 1,738 reportsAug 2024: 1,621 reportsSep 2024: 2,195 reportsOct 2024: 2,234 reportsNov 2024: 2,287 reportsDec 2024: 1,652 reportsJan 2025: 2,404 reportsFeb 2025: 2,344 reportsMar 2025: 2,646 reportsApr 2025: 553 reportsMay 2025: 4 reportsJun 2025: 127 reportsJul 2025: 8,150 reportsAug 2025: 3,073 reportsSep 2025: 1,693 reportsOct 2025: 1,718 reportsNov 2025: 2,256 reportsDec 2025: 2,570 reportsJan 2026: 2,376 reportsFeb 2026: 2,885 reportsMar 2026: 2,483 reportsApr 2026: 2,910 reportsMay 2026: 2,267 reportsJun 2026: 2,012 reportsJul 2026: 2,204 reportsAug 2026: 1,818 reportsSep 2026: 1,087 reportsOct 2026: 0 reports2024202520268,150
Last 36 months. The most recent month may be incomplete.

Most reported NobelActive problems

Device problems

  • Failure to Osseointegrate83,253
  • Loss of Osseointegration48,009
  • Osseointegration Problem8,976
  • Fracture4,702
  • Adverse Event Without Identified Device or Use Problem2,876
  • Patient Device Interaction Problem1,208
  • Migration892
  • Insufficient Device Problem Information524

Patient problems

  • Failure of Implant109,950
  • No Clinical Signs, Symptoms or Conditions31,378
  • Pain17,761
  • Unspecified Infection15,036
  • Numbness2,570
  • Abscess1,665
  • Implant Pain1,249
  • Inflammation1,207

NobelActive models

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

Recent NobelActive adverse event reports

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

Other Nobel Biocare AB products

All Nobel Biocare AB devices →

Sources and updates

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