Lateral Mandibular Angle™ Size: 4/10, RightRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M724TMA0410R1), received between Jun 23, 2022 and Jun 23, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Output Problem” (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

Recent adverse event reports

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

• InjuryJun 23, 2022Output Problem

  THIS IS THE SAME PATIENT ASSOCIATED WITH MDRS # 2028924-2022-00006 AND 2028924-2022-00010. THIS EVENT IS ASSOCIATED WITH RIGHT SIDE MANDIBULAR ANGLE IMPLANT WHICH WAS EXPLANTED APPROXIMATELY 14 MONTHS POST-OP. THOUGH THE DEVICE MAY HAVE BEEN REMOVED PROPHYLACTICALLY DUE TO INFECTION CONCERNS ON THE DEVICE ASSOCIATED WITH MDR # 2028924-2022-00006, THE PATIENT/COMPLAINANT INDICATED THAT THE SURGEONS WHO REMOVED THE DEVICE HAD INDICATED THAT "EVERYTHING WAS OUT OF PLACE AND THE RIGHT SIDE WAS READY TO TEAR THE MUCOSA AND COME TO THE SURFACE."

  Patient problems: Unspecified Infection

  MAUDE report 14788930 ↗