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NobelParallel™ Conical Connection TiUltra™ 300298Recalls & reported problems

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

All models of NobelParallel Conical Connection TiUltra (27)

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

Quick summary

This Nobel Biocare NobelParallel TiUltra dental implant is placed in the jawbone to support a replacement tooth. Of its 6,480 reports, none are deaths and 6,385 are injuries. Many describe the implant failing to bond with the bone, and some note it lacked stability during placement. Some reports mention patients with infection, pain, numbness or abscesses. 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
6,553
Deaths reported
0
Injuries reported
6,458
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6,553 adverse event reports that list this exact device (DI 07332747127904), received between Oct 29, 2021 and Sep 30, 2026 — classified as 6,458 injuries, 95 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (4,870 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Nov 2023: 109 reportsDec 2023: 98 reportsJan 2024: 110 reportsFeb 2024: 143 reportsMar 2024: 99 reportsApr 2024: 126 reportsMay 2024: 96 reportsJun 2024: 86 reportsJul 2024: 66 reportsAug 2024: 62 reportsSep 2024: 154 reportsOct 2024: 146 reportsNov 2024: 80 reportsDec 2024: 87 reportsJan 2025: 100 reportsFeb 2025: 68 reportsMar 2025: 112 reportsApr 2025: 20 reportsMay 2025: 0 reportsJun 2025: 8 reportsJul 2025: 533 reportsAug 2025: 142 reportsSep 2025: 90 reportsOct 2025: 92 reportsNov 2025: 160 reportsDec 2025: 128 reportsJan 2026: 84 reportsFeb 2026: 106 reportsMar 2026: 160 reportsApr 2026: 120 reportsMay 2026: 102 reportsJun 2026: 97 reportsJul 2026: 71 reportsAug 2026: 54 reportsSep 2026: 64 reportsOct 2026: 0 reports202420252026533
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate4,870
  • Loss of Osseointegration727
  • Osseointegration Problem422
  • Adverse Event Without Identified Device or Use Problem162
  • Fracture128
  • Patient Device Interaction Problem84
  • Migration42
  • Activation, Positioning or Separation Problem20

Patient problems

  • Failure of Implant4,396
  • No Clinical Signs, Symptoms or Conditions1,470
  • Pain643
  • Unspecified Infection591
  • Numbness132
  • Abscess131
  • Implant Pain122
  • Inflammation86

Recent adverse event reports

The 25 most recent of 6,553 reports, in the reporter's own words as published by the FDA.

Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices

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Sources and updates

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