Neodent 140.759Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07899878017141), received between Nov 14, 2017 and Sep 23, 2019 — classified as 4 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (4 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.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjurySep 23, 2019Failure to Osseointegrate; Failure to Osseointegrate

  (B)(4) - THE DENTIST REPORTED THAT 4 MONTHS AND 16 DAYS AFTER THE DENTAL IMPLANT WAS INSTALLED IN INTRAORAL REGION 4#, ITS NON- OSSEOINTEGRATION WAS OBSERVED. MOREOVER, 30N.CM OF PRIMARY STABILITY WAS ACHIEVED, THE PATIENT PRESENTED INSUFFICIENT BONE QUALITY/QUANTITY (BONE TYPE III) AND BONE GRAFT WAS PLACED.

  Patient problems: Tissue Damage

  MAUDE report 9106351 ↗
• InjuryDec 7, 2018Failure to Osseointegrate; Failure to Osseointegrate

  (B)(4). THE DENTIST REPORTED THAT 5 MONTHS AFTER THE DENTAL IMPLANT WAS INSTALLED IN INTRAORAL REGION 16#, ITS NON-OSSEOINTEGRATION WAS OBSERVED. IN ADDITION, BONE GRAFT WAS EXECUTED.

  Patient problems: Tissue Damage

  MAUDE report 8143490 ↗
• InjuryAug 29, 2018Failure to Osseointegrate; Failure to Osseointegrate

  (B)(4)¿ THE DENTIST REPORTED THAT ALMOST 6 MONTHS AFTER DENTAL IMPLANT WAS INSTALLED IN INTRAORAL REGION 12#, ITS NON-OSSEOINTEGRATION WAS OBSERVED. 20 NCM OF PRIMARY STABILITY WAS ACHIEVED AND THE PATIENT PRESENTED BONE TYPE III.

  Patient problems: Tissue Damage

  MAUDE report 7828795 ↗
• InjuryNov 14, 2017Failure to Osseointegrate; Failure to Osseointegrate

  (B)(4) ¿ THE DENTIST REPORTED THAT, ONE MONTH AFTER THE DENTAL IMPLANT WAS INSTALLED IN INTRAORAL REGION #8; ITS NON-OSSEOINTEGRATION WAS OBSERVED. TWENTY NCM OF PRIMARY STABILITY WAS ACHIEVED AND IMMEDIATELY LOAD WAS PERFORMED. THE PATIENT PRESENTED BONE TYPE III.

  Patient problems: Tissue Damage

  MAUDE report 7031047 ↗