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IPS 60-000-90-09Recalls & reported problems

KLS-Martin L.P. · IMPLANT, MANDIBLE, 00090, CP TITANIUM · Class 2 · Implant

All models of IPS (29)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888118100917), received between Mar 2, 2018 and Nov 5, 2018 — classified as 2 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 18, 2026.

Most reported problems

Device problems

  • Break2

Patient problems

  • Impaired Healing2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 5, 2018Break; Break

    IT WAS REPORTED THAT A PLATE BROKE. EXPECTED TO BE REMOVED ON AN UNDETERMINED DATE.

    Patient problems: Impaired Healing

    MAUDE report 8039386 ↗
  • InjuryMar 2, 2018Break; Break

    IT WAS REPORTED THAT A PLATE BROKE. THE PLATE WAS REMOVED AND REPLACED. IT IS SUSPECTED THAT THE PATIENT WAS NOT COMPLIANT.

    Patient problems: Impaired Healing

    MAUDE report 7309531 ↗

Other PLATE, BONE devices

All PLATE, BONE devices →

Sources and updates

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