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NobelParallel™ 37966 (UDI 07332747161212)Recalls & reported problems

Nobel Biocare AB · NobelParallel™ Conical Connection NP 3.75x11.5mm · Class 2 · Implant

Quick summary

This Nobel Biocare NobelParallel dental implant has 11,446 adverse event reports, including 11,326 injuries and no deaths. Most describe the implant failing to bond with the jawbone, and patients report implant failure, infection, pain or numbness. A few reports describe fractures. No recalls name this device.

AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.

Adverse event reports
11,587
Deaths reported
0
Injuries reported
11,467
Recalls naming it
0

Summary

The FDA's MAUDE database contains 11,587 adverse event reports that list this exact device (DI 07332747161212), received between Oct 29, 2021 and Sep 30, 2026 — classified as 11,467 injuries, 120 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (8,083 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, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 220 reportsDec 2023: 180 reportsJan 2024: 224 reportsFeb 2024: 211 reportsMar 2024: 255 reportsApr 2024: 222 reportsMay 2024: 204 reportsJun 2024: 211 reportsJul 2024: 197 reportsAug 2024: 193 reportsSep 2024: 245 reportsOct 2024: 192 reportsNov 2024: 229 reportsDec 2024: 125 reportsJan 2025: 213 reportsFeb 2025: 239 reportsMar 2025: 220 reportsApr 2025: 36 reportsMay 2025: 0 reportsJun 2025: 19 reportsJul 2025: 834 reportsAug 2025: 242 reportsSep 2025: 146 reportsOct 2025: 148 reportsNov 2025: 248 reportsDec 2025: 221 reportsJan 2026: 220 reportsFeb 2026: 270 reportsMar 2026: 235 reportsApr 2026: 192 reportsMay 2026: 239 reportsJun 2026: 191 reportsJul 2026: 222 reportsAug 2026: 166 reportsSep 2026: 138 reportsOct 2026: 0 reports202420252026834
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate8,083
  • Loss of Osseointegration2,210
  • Osseointegration Problem692
  • Fracture207
  • Adverse Event Without Identified Device or Use Problem161
  • Patient Device Interaction Problem74
  • Migration38
  • Premature Separation36

Patient problems

  • Failure of Implant7,713
  • No Clinical Signs, Symptoms or Conditions3,059
  • Pain879
  • Unspecified Infection727
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available156
  • Numbness146
  • Abscess129
  • Implant Pain108

Recent adverse event reports

The 25 most recent of 11,587 reports, in the reporter's own words as published by the FDA.

Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices

All IMPLANT, ENDOSSEOUS, ROOT-FORM devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.