Conform Mandibular Angle™ Size: 14, LeftRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M724CMA14L1), received between Oct 19, 2021 and May 25, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMay 25, 2022Malposition of Device

  COMPLAINANT REPORTS PATIENTS RECEIVED MANDIBULAR ANGLE IMPLANTS BILATERALLY AND SUBSEQUENTLY EXPERIENCED DISPLACEMENT, POOR WOUND HEALING AND PAIN THE LEFT SIDE DEVICE WAS EXPLANTED APPROXIMATELY 11 MONTHS POST-OPERATIVELY. (NOTE: THIS IS THE SAME PATIENT ASSOCIATED WITH REPORT # 2028924-2022-00005. THIS REPORT REPRESENTS THE LEFT SIDE DEVICE. REPORT # 2028924-2022-00005 IS THE REPORT FOR THE RIGHT SIDE DEVICE.)

  Patient problems: Impaired Healing; Pain

  MAUDE report 14497809 ↗
• InjuryOct 19, 2021Insufficient Device Problem Information

  COMPLAINANT REPORTED THAT PATIENT WHO HAD MANDIBULAR ANGLE IMPLANTS PLACED, SUBSEQUENTLY HAD IMPLANTS EXPLANTED BILATERALLY APPROXIMATELY 10 WEEKS POST-OPERATIVELY. THIS REPORT IS REGARDING THE LEFT SIDE IMPLANT. (SEE MDR # 2028924-2021-00007 FOR REPORT ON THE RIGHTS SIDE IMPLANT.)

  Patient problems: Insufficient Information

  MAUDE report 12661069 ↗