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IPS 60-000-63-09Recalls & reported problems

KLS-Martin L.P. · IMPLANT, MANDIBLE, 00063, TI-6AL-4V · Class 2 · Implant

All models of IPS (29)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00888118100658), received between Dec 3, 2018 and May 21, 2021 — classified as 3 injuries.

The most frequently reported specific device problem is “Break” (2 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Break2
  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Impaired Healing2
  • Unspecified Infection1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 21, 2021Break; Break

    IT WAS REPORTED A PLATE BROKE. IT WAS REMOVED AND REPLACED.

    Patient problems: Impaired Healing

    MAUDE report 11866985 ↗
  • InjuryMay 14, 2021Break; Break

    IT WAS REPORTED AN IPS PLATE BROKE AND WAS REMOVED.

    Patient problems: Impaired Healing

    MAUDE report 11828623 ↗
  • InjuryDec 3, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PLATE WAS REMOVED DUE TO PATIENT CONDITION.

    Patient problems: Unspecified Infection

    MAUDE report 8126148 ↗

Other PLATE, BONE devices

All PLATE, BONE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page