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NobelParallel Conical Connection TiUltraRecalls & reported problems across all models

Nobel Biocare AB · 27 models in the FDA device registry

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

Adverse event reports
68,868
Deaths reported
0
Injuries reported
68,044
Recalls
0

We found 27 models of NobelParallel Conical Connection TiUltra by Nobel Biocare AB in the FDA's device registry (GUDID). Together they are named in 68,868 adverse event reports in the FDA's MAUDE database, received between Oct 29, 2021 and Sep 30, 2026 — classified as 68,044 injuries, 824 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (49,824 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: 1,399 reportsDec 2023: 972 reportsJan 2024: 1,334 reportsFeb 2024: 1,185 reportsMar 2024: 1,331 reportsApr 2024: 1,473 reportsMay 2024: 1,188 reportsJun 2024: 1,088 reportsJul 2024: 962 reportsAug 2024: 962 reportsSep 2024: 1,397 reportsOct 2024: 1,546 reportsNov 2024: 1,062 reportsDec 2024: 813 reportsJan 2025: 1,055 reportsFeb 2025: 1,133 reportsMar 2025: 1,302 reportsApr 2025: 224 reportsMay 2025: 1 reportsJun 2025: 86 reportsJul 2025: 4,892 reportsAug 2025: 1,407 reportsSep 2025: 974 reportsOct 2025: 916 reportsNov 2025: 1,280 reportsDec 2025: 1,250 reportsJan 2026: 816 reportsFeb 2026: 1,490 reportsMar 2026: 1,379 reportsApr 2026: 1,267 reportsMay 2026: 1,119 reportsJun 2026: 1,193 reportsJul 2026: 1,160 reportsAug 2026: 757 reportsSep 2026: 565 reportsOct 2026: 0 reports2024202520264,892
Last 36 months. The most recent month may be incomplete.

Most reported NobelParallel Conical Connection TiUltra problems

Device problems

  • Failure to Osseointegrate49,824
  • Loss of Osseointegration9,602
  • Osseointegration Problem4,428
  • Adverse Event Without Identified Device or Use Problem1,527
  • Patient Device Interaction Problem904
  • Fracture711
  • Migration409
  • Premature Separation326

Patient problems

  • Failure of Implant46,760
  • No Clinical Signs, Symptoms or Conditions15,100
  • Pain6,286
  • Unspecified Infection5,616
  • Implant Pain1,291
  • Abscess1,101
  • Numbness1,094
  • Inflammation1,089

NobelParallel Conical Connection TiUltra models

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

Recent NobelParallel Conical Connection TiUltra 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