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MIS UNO MO1-11350Recalls & reported problems

MIS Implants Technologies Ltd. · Uno one piece implant dia. 3.50 L 11.50mm · Class 2 · Implant

Quick summary

This MIS Uno dental implant is placed in the jawbone. Reports describe implants that failed to fuse with the bone or were lost, with many reporting dental implant loss. There are 111 reports, all of them injuries, and no deaths, and reports in the last 12 months fell to 0 from 11. 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
111
Deaths reported
0
Injuries reported
111
Recalls naming it
0

Summary

The FDA's MAUDE database contains 111 adverse event reports that list this exact device (DI 07290108995824), received between Aug 8, 2024 and Feb 13, 2025 — classified as 111 injuries.

The most frequently reported specific device problem is “Osseointegration Problem” (100 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: 55 reportsSep 2024: 45 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 1 reportsFeb 2025: 10 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports20242025202655
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Osseointegration Problem100
  • Failure to Osseointegrate11

Patient problems

  • Failure of Implant111

Recent adverse event reports

The 25 most recent of 111 reports, in the reporter's own words as published by the FDA.

  • InjuryFeb 13, 2025Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 21372795 ↗
  • InjuryFeb 12, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IMPLANT FAILURE.

    Patient problems: Failure of Implant

    MAUDE report 21366781 ↗
  • InjuryFeb 12, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IMPLANT FAILURE.

    Patient problems: Failure of Implant

    MAUDE report 21366769 ↗
  • InjuryFeb 12, 2025Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 21366767 ↗
  • InjuryFeb 9, 2025Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 21340899 ↗
  • InjuryFeb 9, 2025Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 21340881 ↗
  • InjuryFeb 9, 2025Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 21340867 ↗
  • InjuryFeb 5, 2025Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 21311483 ↗
  • InjuryFeb 4, 2025Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 21309133 ↗
  • InjuryFeb 4, 2025Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 21308875 ↗
  • InjuryJan 31, 2025Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 21282770 ↗
  • InjurySep 23, 2024Osseointegration Problem; Osseointegration Problem

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

    Patient problems: Failure of Implant

    MAUDE report 20278771 ↗
  • InjurySep 20, 2024Osseointegration Problem; Osseointegration Problem

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

    Patient problems: Failure of Implant

    MAUDE report 20264538 ↗
  • InjurySep 19, 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 20259413 ↗
  • InjurySep 19, 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 20259077 ↗
  • InjurySep 18, 2024Osseointegration Problem; Osseointegration Problem

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

    Patient problems: Failure of Implant

    MAUDE report 20246706 ↗
  • InjurySep 18, 2024Osseointegration Problem; Osseointegration Problem

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

    Patient problems: Failure of Implant

    MAUDE report 20243695 ↗
  • InjurySep 18, 2024Osseointegration Problem; Osseointegration Problem

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS. DAY OF SURGERY/0-4 WEEKS FROM SURGERY.

    Patient problems: Failure of Implant

    MAUDE report 20243636 ↗
  • InjurySep 18, 2024Osseointegration Problem; Osseointegration Problem

    IT WAS REPORTED, THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS. DAY OF SURGERY, 0-4 WEEKS FROM SURGERY.

    Patient problems: Failure of Implant

    MAUDE report 20243566 ↗
  • InjurySep 15, 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 20220851 ↗
  • InjurySep 15, 2024Osseointegration Problem; Osseointegration Problem

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS. DAY OF SURGERY/0-4 WEEKS FROM SURGERY.

    Patient problems: Failure of Implant

    MAUDE report 20220122 ↗
  • InjurySep 11, 2024Osseointegration Problem; Osseointegration Problem

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

    Patient problems: Failure of Implant

    MAUDE report 20191096 ↗
  • InjurySep 11, 2024Osseointegration Problem; Osseointegration Problem

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

    Patient problems: Failure of Implant

    MAUDE report 20190869 ↗
  • InjurySep 10, 2024Osseointegration Problem; Osseointegration Problem

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

    Patient problems: Failure of Implant

    MAUDE report 20178302 ↗
  • InjurySep 10, 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 20178264 ↗

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.