Skip to content

MIS MF7-D10500Recalls & reported problems

MIS Implants Technologies Ltd. · SEVEN XD int. hex. implant D5 L10mm WP · Class 2 · Implant

Quick summary

This MIS Seven XD dental implant is a post placed in the jawbone to hold a replacement tooth. Most of its 465 reports describe the implant failing to bond with the bone or being lost. The reports include 464 injuries and no deaths, and reports in the last 12 months fell to 159 from 255 before. 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
502
Deaths reported
0
Injuries reported
501
Recalls naming it
0

Summary

The FDA's MAUDE database contains 502 adverse event reports that list this exact device (DI 07290113997745), received between May 19, 2023 and Sep 30, 2026 — classified as 501 injuries, 1 malfunction.

The most frequently reported specific device problem is “Failure to Osseointegrate” (374 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: 7 reportsSep 2024: 16 reportsOct 2024: 27 reportsNov 2024: 36 reportsDec 2024: 30 reportsJan 2025: 18 reportsFeb 2025: 23 reportsMar 2025: 14 reportsApr 2025: 21 reportsMay 2025: 24 reportsJun 2025: 26 reportsJul 2025: 21 reportsAug 2025: 13 reportsSep 2025: 14 reportsOct 2025: 15 reportsNov 2025: 8 reportsDec 2025: 24 reportsJan 2026: 18 reportsFeb 2026: 27 reportsMar 2026: 11 reportsApr 2026: 10 reportsMay 2026: 21 reportsJun 2026: 14 reportsJul 2026: 17 reportsAug 2026: 8 reportsSep 2026: 38 reportsOct 2026: 0 reports20242025202638
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate374
  • Osseointegration Problem90
  • Loss of Osseointegration36
  • Malposition of Device1
  • Material Deformation1

Patient problems

  • Failure of Implant463
  • No Clinical Signs, Symptoms or Conditions33
  • Inadequate Osseointegration5
  • Osteolysis1
  • Sinus Perforation1
  • Unspecified Infection1

Recent adverse event reports

The 25 most recent of 502 reports, in the reporter's own words as published by the FDA.

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.