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NobelParallel™ 37967 (UDI 07332747161229)Recalls & reported problems

Nobel Biocare AB · NobelParallel™ Conical Connection NP 3.75x13mm · Class 2 · Implant

Quick summary

This Nobel Biocare NobelParallel dental implant is placed in the jawbone. The reports mostly describe implants that failed to bond with the bone, with some also mentioning pain, infection or numbness. FDA records list 5,800 reports, no deaths, 5,739 injuries and 61 malfunctions. 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
5,873
Deaths reported
0
Injuries reported
5,812
Recalls naming it
0

Summary

The FDA's MAUDE database contains 5,873 adverse event reports that list this exact device (DI 07332747161229), received between Oct 29, 2021 and Sep 30, 2026 — classified as 5,812 injuries, 61 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (4,025 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: 129 reportsDec 2023: 112 reportsJan 2024: 96 reportsFeb 2024: 93 reportsMar 2024: 118 reportsApr 2024: 80 reportsMay 2024: 101 reportsJun 2024: 81 reportsJul 2024: 117 reportsAug 2024: 91 reportsSep 2024: 105 reportsOct 2024: 118 reportsNov 2024: 111 reportsDec 2024: 57 reportsJan 2025: 109 reportsFeb 2025: 111 reportsMar 2025: 111 reportsApr 2025: 2 reportsMay 2025: 1 reportsJun 2025: 10 reportsJul 2025: 397 reportsAug 2025: 125 reportsSep 2025: 78 reportsOct 2025: 88 reportsNov 2025: 126 reportsDec 2025: 124 reportsJan 2026: 120 reportsFeb 2026: 164 reportsMar 2026: 104 reportsApr 2026: 112 reportsMay 2026: 86 reportsJun 2026: 82 reportsJul 2026: 97 reportsAug 2026: 93 reportsSep 2026: 70 reportsOct 2026: 0 reports202420252026397
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate4,025
  • Loss of Osseointegration1,167
  • Osseointegration Problem345
  • Adverse Event Without Identified Device or Use Problem109
  • Fracture89
  • Patient Device Interaction Problem38
  • Migration33
  • Activation, Positioning or Separation Problem13

Patient problems

  • Failure of Implant3,922
  • No Clinical Signs, Symptoms or Conditions1,566
  • Pain477
  • Unspecified Infection402
  • Numbness90
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available69
  • Abscess57
  • Fistula49

Recent adverse event reports

The 25 most recent of 5,873 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.