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Z-Max Implant System Z-MAX8-9Recalls & reported problems

Keystone Dental, Inc. · Implant · Class 2 · Implant

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 D768ZMAX890), received between May 31, 2022 and Jun 28, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (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 18, 2026.

Most reported problems

Device problems

  • Failure to Osseointegrate1
  • Loss of Osseointegration1

Patient problems

  • Bacterial Infection2

Recent adverse event reports

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

  • InjuryJun 28, 2022Failure to Osseointegrate; Failure to Osseointegrate

    FAILED TO OSSEOINTEGRATE.

    Patient problems: Bacterial Infection

    MAUDE report 14843175 ↗
  • InjuryMay 31, 2022Loss of Osseointegration; Loss of Osseointegration

    LOSS OF OSSEOINTEGRATION.

    Patient problems: Bacterial Infection

    MAUDE report 14548690 ↗

Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices

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Sources and updates

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