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MIS MF5-08600Recalls & reported problems

MIS Implants Technologies Ltd. · Lance internal hex. implant dia. 6 L 8mm · Class 2 · Implant

Quick summary

This MIS Implants root-form dental implant is the subject of 28 adverse event reports. The reports mostly describe the implant failing to bond with the surrounding bone, which led to the implant being lost. All 28 reports involve injuries, and there are no deaths. No recalls name this device. Reports dropped sharply, from 26 in the previous 12 months to 1 in the last 12 months.

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
29
Deaths reported
0
Injuries reported
29
Recalls naming it
0

Summary

The FDA's MAUDE database contains 29 adverse event reports that list this exact device (DI 07290113995604), received between Aug 25, 2024 and Sep 12, 2026 — classified as 29 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (23 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: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 1 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 4 reportsDec 2024: 2 reportsJan 2025: 0 reportsFeb 2025: 9 reportsMar 2025: 1 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 8 reportsJul 2025: 1 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 1 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 1 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 1 reportsOct 2026: 0 reports2024202520269
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate23
  • Osseointegration Problem6

Patient problems

  • Failure of Implant28
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 25 most recent of 29 reports, in the reporter's own words as published by the FDA.

  • InjurySep 12, 2026Failure to Osseointegrate

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50745787 ↗
  • InjuryFeb 26, 2026Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 24465889 ↗
  • InjuryOct 25, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 23386838 ↗
  • InjuryJul 29, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22641480 ↗
  • InjuryJun 11, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22189114 ↗
  • InjuryJun 11, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22187062 ↗
  • InjuryJun 11, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22186773 ↗
  • InjuryJun 11, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22186542 ↗
  • InjuryJun 11, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22183809 ↗
  • InjuryJun 11, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22183777 ↗
  • InjuryJun 11, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22183622 ↗
  • InjuryJun 10, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 22178841 ↗
  • InjuryMar 6, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21541022 ↗
  • InjuryFeb 11, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21357931 ↗
  • InjuryFeb 11, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21357841 ↗
  • InjuryFeb 7, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21332634 ↗
  • InjuryFeb 6, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21322638 ↗
  • InjuryFeb 6, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21322400 ↗
  • InjuryFeb 6, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21322231 ↗
  • InjuryFeb 6, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21321842 ↗
  • InjuryFeb 6, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21321817 ↗
  • InjuryFeb 6, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21321729 ↗
  • InjuryDec 26, 2024Failure to Osseointegrate; Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 21021734 ↗
  • InjuryDec 3, 2024Osseointegration Problem; Osseointegration Problem

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS. LESS THEN 4 MONTHS FROM SURGERY.

    Patient problems: Failure of Implant

    MAUDE report 20835333 ↗
  • InjuryNov 28, 2024Osseointegration Problem; Osseointegration Problem

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS. MORE THAN 4 MONTHS FROM SURGERY.

    Patient problems: Failure of Implant

    MAUDE report 20808228 ↗

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.