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MIS C1 C1-13420Recalls & reported problems

MIS Implants Technologies Ltd. · C1 coni con implant D4.20 L13mm, SP · Class 2 · Implant

Quick summary

This MIS C1 dental implant appears in 674 adverse event reports, with no deaths and 674 injuries. Reports mostly describe the implant failing to fuse with the jawbone and being lost, with some also noting infection. Reports fell over the last 12 months, to 122 from 400 in the 12 months before, and there are no recalls that 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
686
Deaths reported
0
Injuries reported
686
Recalls naming it
0

Summary

The FDA's MAUDE database contains 686 adverse event reports that list this exact device (DI 07290108992045), received between Aug 13, 2024 and Sep 29, 2026 — classified as 686 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (420 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: 30 reportsSep 2024: 51 reportsOct 2024: 71 reportsNov 2024: 57 reportsDec 2024: 60 reportsJan 2025: 46 reportsFeb 2025: 58 reportsMar 2025: 46 reportsApr 2025: 6 reportsMay 2025: 24 reportsJun 2025: 39 reportsJul 2025: 13 reportsAug 2025: 29 reportsSep 2025: 4 reportsOct 2025: 18 reportsNov 2025: 10 reportsDec 2025: 21 reportsJan 2026: 7 reportsFeb 2026: 20 reportsMar 2026: 10 reportsApr 2026: 5 reportsMay 2026: 8 reportsJun 2026: 23 reportsJul 2026: 1 reportsAug 2026: 17 reportsSep 2026: 12 reportsOct 2026: 0 reports20242025202671
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate420
  • Osseointegration Problem254
  • Loss of Osseointegration12

Patient problems

  • Failure of Implant674
  • No Clinical Signs, Symptoms or Conditions6
  • Inadequate Osseointegration5
  • Insufficient Information1

Recent adverse event reports

The 25 most recent of 686 reports, in the reporter's own words as published by the FDA.

  • 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 50937314 ↗
  • 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 50915120 ↗
  • InjurySep 15, 2026Loss of Osseointegration

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

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50778363 ↗
  • InjurySep 15, 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 50774302 ↗
  • InjurySep 11, 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 50734667 ↗
  • InjurySep 11, 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 50734319 ↗
  • InjurySep 10, 2026Loss of Osseointegration

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

    Patient problems: Inadequate Osseointegration

    MAUDE report 50720627 ↗
  • InjurySep 10, 2026Loss of Osseointegration

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

    Patient problems: Inadequate Osseointegration

    MAUDE report 50718134 ↗
  • InjurySep 10, 2026Loss of Osseointegration

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

    Patient problems: Inadequate Osseointegration

    MAUDE report 50718047 ↗
  • InjurySep 10, 2026Loss of Osseointegration

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

    Patient problems: Inadequate Osseointegration

    MAUDE report 50716772 ↗
  • InjurySep 10, 2026Loss of Osseointegration

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

    Patient problems: Insufficient Information

    MAUDE report 50715903 ↗
  • InjurySep 9, 2026Loss of Osseointegration

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

    Patient problems: Inadequate Osseointegration

    MAUDE report 50692812 ↗
  • InjuryAug 16, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant loss. Also, it was reported that they had unspecified infection.

    Patient problems: Failure of Implant

    MAUDE report 50267587 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217799 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217798 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217795 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217794 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217792 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217773 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217771 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217769 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217767 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217764 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217762 ↗
  • InjuryAug 12, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50217759 ↗

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.