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Neodent 109.219Recalls & reported problems

JJGC Indústria e Comércio de Materiais Dentários S/A. · ALVIM IMPLANT WITH MOUNT · Class 2 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07898237566825), received between Jan 22, 2020 and Jan 22, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Failure to Osseointegrate” (1 report).

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 16, 2026.

Most reported problems

Device problems

  • Failure to Osseointegrate1

Patient problems

  • Tissue Damage1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 22, 2020Failure to Osseointegrate; Failure to Osseointegrate

    (B)(4) ¿ THE DENTIST REPORTED THAT 1 MONTH AFTER THE DENTAL IMPLANT WAS INSTALLED IN PATIENT¿S MOUTH, ITS NON-OSSEOINTEGRATION WAS OBSERVED. MOREOVER, THE PATIENT PRESENTED BONE TYPE II, IMMEDIATE IMPLANT WAS PERFORMED, BONE GRAFT WAS PLACED AND BIOMECHANICAL OVERLOAD HAS OCCURRED.

    Patient problems: Tissue Damage

    MAUDE report 9616988 ↗

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Sources and updates

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