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MIS C1 C1-08420Recalls & reported problems

MIS Implants Technologies Ltd. · C1 coni con implant D4.20 L8mm SP · Class 2 · Implant

Quick summary

This MIS C1 dental implant is a screw placed in the jawbone to hold a replacement tooth. Most reports describe the implant being lost or failing to bond with the bone. The records include 1,965 reports and 1,965 injuries, with no deaths, and no recalls name this device. Reports fell from 1,225 in the year before to 380 in the most recent year.

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
1,983
Deaths reported
0
Injuries reported
1,983
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1,983 adverse event reports that list this exact device (DI 07290108992021), received between Aug 8, 2024 and Sep 29, 2026 — classified as 1,983 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (1,262 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: 76 reportsSep 2024: 119 reportsOct 2024: 165 reportsNov 2024: 208 reportsDec 2024: 168 reportsJan 2025: 32 reportsFeb 2025: 217 reportsMar 2025: 186 reportsApr 2025: 28 reportsMay 2025: 54 reportsJun 2025: 104 reportsJul 2025: 90 reportsAug 2025: 100 reportsSep 2025: 3 reportsOct 2025: 35 reportsNov 2025: 48 reportsDec 2025: 55 reportsJan 2026: 10 reportsFeb 2026: 54 reportsMar 2026: 23 reportsApr 2026: 25 reportsMay 2026: 34 reportsJun 2026: 75 reportsJul 2026: 18 reportsAug 2026: 38 reportsSep 2026: 18 reportsOct 2026: 0 reports202420252026217
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate1,262
  • Osseointegration Problem707
  • Loss of Osseointegration14

Patient problems

  • Failure of Implant1,962
  • No Clinical Signs, Symptoms or Conditions17
  • Insufficient Information3
  • Inadequate Osseointegration2
  • Osteolysis2

Recent adverse event reports

The 25 most recent of 1,983 reports, in the reporter's own words as published by the FDA.

  • InjurySep 29, 2026Loss of Osseointegration

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50937679 ↗
  • InjurySep 16, 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 50788605 ↗
  • 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 50773291 ↗
  • InjurySep 10, 2026Loss of Osseointegration

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50722334 ↗
  • InjurySep 10, 2026Loss of Osseointegration

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

    Patient problems: Insufficient Information

    MAUDE report 50717838 ↗
  • InjurySep 10, 2026Loss of Osseointegration

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

    Patient problems: Inadequate Osseointegration

    MAUDE report 50717723 ↗
  • InjurySep 10, 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 50715262 ↗
  • InjurySep 10, 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 50715258 ↗
  • InjurySep 10, 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 50715207 ↗
  • InjurySep 10, 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 50715185 ↗
  • InjurySep 10, 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 50715128 ↗
  • InjurySep 10, 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 50715017 ↗
  • InjurySep 10, 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 50715001 ↗
  • InjurySep 10, 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 50714924 ↗
  • InjurySep 10, 2026Loss of Osseointegration

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

    Patient problems: Insufficient Information

    MAUDE report 50714577 ↗
  • InjurySep 9, 2026Loss of Osseointegration

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

    Patient problems: Insufficient Information

    MAUDE report 50690340 ↗
  • InjurySep 8, 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 50675474 ↗
  • InjurySep 8, 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 50674482 ↗
  • InjuryAug 25, 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 50434462 ↗
  • InjuryAug 25, 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 50434371 ↗
  • InjuryAug 24, 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 50412017 ↗
  • InjuryAug 24, 2026Loss of Osseointegration

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

    Patient problems: Failure of Implant; Osteolysis

    MAUDE report 50406160 ↗
  • InjuryAug 24, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant; Inadequate Osseointegration

    MAUDE report 50405534 ↗
  • InjuryAug 16, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50267371 ↗
  • InjuryAug 14, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50256539 ↗

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.