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MIS C1 C1-11330Recalls & reported problems

MIS Implants Technologies Ltd. · C1 coni. con. implant D3.30 L11.5mm, NP · Class 2 · Implant

Quick summary

This MIS C1 is a root-form dental implant placed in the jawbone. Of the 608 reports naming it, most describe the implant failing to fuse with the bone, with many patients losing it and some mentioning infection. The reports include 608 injuries and no deaths, and reports fell from 376 in the previous 12 months to 79 in the latest 12 months. No recalls 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
613
Deaths reported
0
Injuries reported
613
Recalls naming it
0

Summary

The FDA's MAUDE database contains 613 adverse event reports that list this exact device (DI 07290108992137), received between Aug 8, 2024 and Sep 30, 2026 — classified as 613 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (360 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: 38 reportsSep 2024: 60 reportsOct 2024: 55 reportsNov 2024: 64 reportsDec 2024: 58 reportsJan 2025: 47 reportsFeb 2025: 31 reportsMar 2025: 55 reportsApr 2025: 7 reportsMay 2025: 18 reportsJun 2025: 32 reportsJul 2025: 25 reportsAug 2025: 19 reportsSep 2025: 4 reportsOct 2025: 16 reportsNov 2025: 13 reportsDec 2025: 9 reportsJan 2026: 7 reportsFeb 2026: 8 reportsMar 2026: 7 reportsApr 2026: 6 reportsMay 2026: 9 reportsJun 2026: 8 reportsJul 2026: 6 reportsAug 2026: 6 reportsSep 2026: 5 reportsOct 2026: 0 reports20242025202664
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate360
  • Osseointegration Problem247
  • Loss of Osseointegration5
  • Loosening of Implant Not Related to Bone-Ingrowth1

Patient problems

  • Failure of Implant608
  • No Clinical Signs, Symptoms or Conditions4
  • Inflammation1
  • Insufficient Information1

Recent adverse event reports

The 25 most recent of 613 reports, in the reporter's own words as published by the FDA.

  • InjurySep 30, 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 50944172 ↗
  • InjurySep 30, 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 50944104 ↗
  • InjurySep 30, 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 50944012 ↗
  • InjurySep 11, 2026Loss of Osseointegration

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50740389 ↗
  • InjurySep 10, 2026Loss of Osseointegration

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

    Patient problems: Insufficient Information

    MAUDE report 50714745 ↗
  • InjuryAug 14, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50253321 ↗
  • InjuryAug 13, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50235143 ↗
  • InjuryAug 11, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant failure;Soft bone in the placement area. Latent pain during the osseointegration process.

    Patient problems: Failure of Implant

    MAUDE report 50203226 ↗
  • InjuryAug 11, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant failure;"Postoperative infection 1 month after implant placement, diabetic patient."

    Patient problems: Failure of Implant

    MAUDE report 50203151 ↗
  • InjuryAug 10, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 50194125 ↗
  • InjuryAug 5, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant loss with periimplantitis and bone resorption.

    Patient problems: Failure of Implant; Inflammation

    MAUDE report 50141524 ↗
  • InjuryJul 27, 2026Failure to Osseointegrate

    It was reported that a patient experienced a dental implant loss due to peri-implantitis.

    Patient problems: Failure of Implant

    MAUDE report 50034782 ↗
  • InjuryJul 14, 2026Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS DUE TO INFECTION.

    Patient problems: Failure of Implant

    MAUDE report 25818611 ↗
  • InjuryJul 13, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 25797501 ↗
  • InjuryJul 8, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 25749625 ↗
  • InjuryJul 7, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 25733350 ↗
  • InjuryJul 1, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 25681802 ↗
  • InjuryJun 18, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 25549845 ↗
  • InjuryJun 17, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 25538962 ↗
  • InjuryJun 17, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 25538959 ↗
  • InjuryJun 17, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 25538957 ↗
  • InjuryJun 17, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 25538934 ↗
  • InjuryJun 17, 2026Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 25538932 ↗
  • InjuryJun 12, 2026Loosening of Implant Not Related to Bone-Ingrowth

    IT WAS REPORTED THAT THE IMPLANT BRIDGE HAS WORN THE INSIDE OF THE IMPLANT, RESULTING IN IMPLANT LOSS.

    Patient problems: Failure of Implant

    MAUDE report 25485891 ↗
  • InjuryJun 10, 2026Failure to Osseointegrate

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS. NO OSSEOINTEGRATED.

    Patient problems: Failure of Implant

    MAUDE report 25462299 ↗

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.