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NobelParallelRecalls & reported problems across all models

Nobel Biocare AB · 54 models in the FDA device registry

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

Adverse event reports
132,525
Deaths reported
1
Injuries reported
131,604
Recalls
0

We found 54 models of NobelParallel by Nobel Biocare AB in the FDA's device registry (GUDID). Together they are named in 132,525 adverse event reports in the FDA's MAUDE database, received between Jun 1, 2018 and Sep 30, 2026 — classified as 1 death, 131,604 injuries, 920 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (83,452 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: 2,279 reportsDec 2023: 2,175 reportsJan 2024: 2,205 reportsFeb 2024: 2,115 reportsMar 2024: 2,327 reportsApr 2024: 2,222 reportsMay 2024: 2,035 reportsJun 2024: 2,051 reportsJul 2024: 1,819 reportsAug 2024: 1,629 reportsSep 2024: 2,058 reportsOct 2024: 2,145 reportsNov 2024: 2,161 reportsDec 2024: 1,562 reportsJan 2025: 2,221 reportsFeb 2025: 2,166 reportsMar 2025: 2,312 reportsApr 2025: 425 reportsMay 2025: 2 reportsJun 2025: 218 reportsJul 2025: 8,165 reportsAug 2025: 2,671 reportsSep 2025: 1,621 reportsOct 2025: 1,774 reportsNov 2025: 2,448 reportsDec 2025: 2,387 reportsJan 2026: 2,382 reportsFeb 2026: 2,778 reportsMar 2026: 2,414 reportsApr 2026: 2,342 reportsMay 2026: 2,305 reportsJun 2026: 1,955 reportsJul 2026: 2,456 reportsAug 2026: 1,838 reportsSep 2026: 1,217 reportsOct 2026: 0 reports2024202520268,165
Last 36 months. The most recent month may be incomplete.

Most reported NobelParallel problems

Device problems

  • Failure to Osseointegrate83,452
  • Loss of Osseointegration36,521
  • Osseointegration Problem6,939
  • Adverse Event Without Identified Device or Use Problem1,641
  • Fracture1,566
  • Patient Device Interaction Problem794
  • Migration452
  • Premature Separation288

Patient problems

  • Failure of Implant92,123
  • No Clinical Signs, Symptoms or Conditions31,684
  • Pain11,805
  • Unspecified Infection8,639
  • Numbness2,276
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1,740
  • Implant Pain1,124
  • Abscess1,034

NobelParallel models

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

Recent NobelParallel 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