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NobelSpeedyRecalls & reported problems across all models

Nobel Biocare AB · 88 models in the FDA device registry

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

Adverse event reports
24,246
Deaths reported
1
Injuries reported
24,075
Recalls
0

We found 88 models of NobelSpeedy by Nobel Biocare AB in the FDA's device registry (GUDID). Together they are named in 24,246 adverse event reports in the FDA's MAUDE database, received between Sep 10, 2019 and Sep 30, 2026 — classified as 1 death, 24,075 injuries, 170 malfunctions.

The most frequently reported specific device problem is “Loss of Osseointegration” (12,964 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: 450 reportsDec 2023: 404 reportsJan 2024: 315 reportsFeb 2024: 561 reportsMar 2024: 399 reportsApr 2024: 384 reportsMay 2024: 352 reportsJun 2024: 322 reportsJul 2024: 380 reportsAug 2024: 140 reportsSep 2024: 322 reportsOct 2024: 389 reportsNov 2024: 304 reportsDec 2024: 293 reportsJan 2025: 221 reportsFeb 2025: 382 reportsMar 2025: 396 reportsApr 2025: 62 reportsMay 2025: 1 reportsJun 2025: 18 reportsJul 2025: 1,002 reportsAug 2025: 470 reportsSep 2025: 232 reportsOct 2025: 360 reportsNov 2025: 404 reportsDec 2025: 379 reportsJan 2026: 331 reportsFeb 2026: 358 reportsMar 2026: 277 reportsApr 2026: 322 reportsMay 2026: 350 reportsJun 2026: 288 reportsJul 2026: 327 reportsAug 2026: 110 reportsSep 2026: 240 reportsOct 2026: 0 reports2024202520261,002
Last 36 months. The most recent month may be incomplete.

Most reported NobelSpeedy problems

Device problems

  • Loss of Osseointegration12,964
  • Failure to Osseointegrate9,068
  • Osseointegration Problem930
  • Adverse Event Without Identified Device or Use Problem371
  • Fracture330
  • Patient Device Interaction Problem304
  • Premature Separation54
  • Migration44

Patient problems

  • Failure of Implant18,351
  • Pain3,627
  • Unspecified Infection3,179
  • No Clinical Signs, Symptoms or Conditions3,148
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available921
  • Numbness714
  • Abscess304
  • Inflammation153

NobelSpeedy models

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

Recent NobelSpeedy 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