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Kyocera Medical Technologies, Inc. S 150 (REF 1055-161-307)Recalls & reported problems

Kyocera Medical Technologies, Inc. · SA Cervical Cage, 16mm x 13.5mm x 7mm, 7° Lordosis, T3 · Class 2 · Implant

Data updated Oct 18, 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 00841523118267), received between Nov 26, 2019 and Nov 26, 2019 — classified as 1 injury.

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
  • Migration1

Patient problems

  • Failure of Implant1
  • Inadequate Osseointegration1

Recent adverse event reports

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

  • InjuryNov 26, 2019Failure to Osseointegrate; Migration; Failure to Osseointegrate; Migration

    A COMPLAINT WAS RECEIVED WHICH STATED THAT A CERVICAL CAGE SUBSIDED 3 YEARS POST OPERATION. THE CERVICAL COVER PLATE AND A SCREW WERE ALSO FOUND TO HAVE FRACTURED, WHICH CAUSED THE COVER PLATE TO PROTRUDE. THIS WAS DISCOVERED DURING FOLLOW-UP VISIT TO THE SURGEON, PATIENT WAS ASYMPTOMATIC AT THE TIME OF DISCOVERY.

    Patient problems: Failure of Implant; Inadequate Osseointegration

    MAUDE report 9379327 ↗

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Sources and updates

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