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MIS MF5-10420Recalls & reported problems

MIS Implants Technologies Ltd. · Lance internal hex. implant dia. 4.20 L 10mm · Class 2 · Implant

Quick summary

This MIS Lance dental implant is a root-form implant placed in the jawbone. Its 3,215 reports mostly describe the implant failing to fuse with the jawbone, with patients reporting that the implant was lost. The reports include no deaths and 3,215 injuries. No recalls name this device. Reports fell sharply in the most recent year (871) from the year before (1,866).

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
3,299
Deaths reported
0
Injuries reported
3,299
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3,299 adverse event reports that list this exact device (DI 07290113995635), received between Aug 8, 2024 and Sep 30, 2026 — classified as 3,299 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (2,054 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: 91 reportsSep 2024: 262 reportsOct 2024: 125 reportsNov 2024: 341 reportsDec 2024: 436 reportsJan 2025: 164 reportsFeb 2025: 107 reportsMar 2025: 53 reportsApr 2025: 28 reportsMay 2025: 91 reportsJun 2025: 58 reportsJul 2025: 294 reportsAug 2025: 146 reportsSep 2025: 106 reportsOct 2025: 42 reportsNov 2025: 63 reportsDec 2025: 112 reportsJan 2026: 72 reportsFeb 2026: 124 reportsMar 2026: 142 reportsApr 2026: 121 reportsMay 2026: 79 reportsJun 2026: 93 reportsJul 2026: 40 reportsAug 2026: 25 reportsSep 2026: 84 reportsOct 2026: 0 reports202420252026436
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate2,054
  • Osseointegration Problem1,182
  • Loss of Osseointegration61
  • Fracture2

Patient problems

  • Failure of Implant3,215
  • No Clinical Signs, Symptoms or Conditions41
  • Unspecified Infection38
  • Inadequate Osseointegration30
  • Inflammation19
  • Osteolysis2
  • Deformity/ Disfigurement1
  • Tissue Breakdown1

Recent adverse event reports

The 25 most recent of 3,299 reports, in the reporter's own words as published by the FDA.

  • InjurySep 30, 2026Failure to Osseointegrate

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50952450 ↗
  • InjurySep 29, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50936964 ↗
  • InjurySep 29, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50936962 ↗
  • InjurySep 29, 2026Failure to Osseointegrate

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50936926 ↗
  • InjurySep 29, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50930756 ↗
  • InjurySep 29, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50930716 ↗
  • InjurySep 29, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50930647 ↗
  • InjurySep 29, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50930636 ↗
  • InjurySep 29, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50930632 ↗
  • InjurySep 29, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50930620 ↗
  • InjurySep 28, 2026Failure to Osseointegrate

    Patient problems: Inadequate Osseointegration

    MAUDE report 50926211 ↗
  • InjurySep 28, 2026Failure to Osseointegrate

    Patient problems: Inadequate Osseointegration

    MAUDE report 50925992 ↗
  • InjurySep 28, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50916690 ↗
  • InjurySep 28, 2026Loss of Osseointegration

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50916684 ↗
  • InjurySep 21, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50837628 ↗
  • InjurySep 21, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50837620 ↗
  • InjurySep 21, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50837589 ↗
  • InjurySep 21, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50837574 ↗
  • InjurySep 21, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50837569 ↗
  • InjurySep 20, 2026Failure to Osseointegrate

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50834917 ↗
  • InjurySep 18, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50820990 ↗
  • InjurySep 18, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50820015 ↗
  • InjurySep 18, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50818601 ↗
  • InjurySep 18, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50818535 ↗
  • InjurySep 18, 2026Loss of Osseointegration

    It was reported that a patient experienced a dental implant loss. There was no reported injury.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50818526 ↗

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.