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IPS 60-000-72-09Recalls & reported problems

KLS-Martin L.P. · IMPLANT, MIDFACE/ORTHOG, 00072, 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
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888118100740), received between Jun 19, 2017 and Jun 19, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (1 report).

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

  • Fracture1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 19, 2017Fracture; Fracture

    IT WAS REPORTED THE IPS ORTHOGNATHIC PLATE BROKE DURING PLACEMENT. A BACK UP PLATE WAS AVAILABLE TO REPLACE THE BROKEN PLATE AND THE CASE WAS COMPLETED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6649534 ↗

Other PLATE, BONE devices

All PLATE, BONE devices →

Sources and updates

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