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NobelReplace® 36710 (UDI 07332747160550)Recalls & reported problems

Nobel Biocare AB · NobelReplace® Conical Connection RP 5.0x8mm · Class 2 · Implant

Quick summary

This NobelReplace dental implant from Nobel Biocare is placed in the jawbone to support a replacement tooth. Most reports describe the implant failing to fuse with the bone or later losing that connection, and some describe the implant itself failing. The 3,779 reports include 3,750 injuries and no deaths. 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
3,883
Deaths reported
0
Injuries reported
3,854
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3,883 adverse event reports that list this exact device (DI 07332747160550), received between Oct 29, 2021 and Sep 30, 2026 — classified as 3,854 injuries, 29 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (2,889 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: 39 reportsDec 2023: 41 reportsJan 2024: 43 reportsFeb 2024: 27 reportsMar 2024: 50 reportsApr 2024: 33 reportsMay 2024: 30 reportsJun 2024: 48 reportsJul 2024: 41 reportsAug 2024: 43 reportsSep 2024: 56 reportsOct 2024: 71 reportsNov 2024: 88 reportsDec 2024: 96 reportsJan 2025: 154 reportsFeb 2025: 54 reportsMar 2025: 116 reportsApr 2025: 26 reportsMay 2025: 0 reportsJun 2025: 8 reportsJul 2025: 484 reportsAug 2025: 152 reportsSep 2025: 80 reportsOct 2025: 62 reportsNov 2025: 106 reportsDec 2025: 124 reportsJan 2026: 128 reportsFeb 2026: 82 reportsMar 2026: 112 reportsApr 2026: 114 reportsMay 2026: 106 reportsJun 2026: 98 reportsJul 2026: 119 reportsAug 2026: 81 reportsSep 2026: 101 reportsOct 2026: 0 reports202420252026484
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate2,889
  • Loss of Osseointegration687
  • Osseointegration Problem198
  • Adverse Event Without Identified Device or Use Problem41
  • Patient Device Interaction Problem28
  • Insufficient Device Problem Information12
  • Fracture7
  • Migration6

Patient problems

  • Failure of Implant1,882
  • No Clinical Signs, Symptoms or Conditions1,550
  • Unspecified Infection396
  • Pain126
  • Inflammation82
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available46
  • Implant Pain30
  • Numbness30

Recent adverse event reports

The 25 most recent of 3,883 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.