Terino Square Chin-Style II Size: X-LargeRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M724TSCIIXL1), received between Oct 8, 2021 and Oct 8, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

1 other recall cover devices cleared under the same FDA submission (K902824); they may or may not involve this specific model.

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.

• InjuryOct 8, 2021Device Dislodged or Dislocated

  COMPLAINANT REPORTED THAT PATIENT WHO HAD INTRAORAL PLACEMENT OF A CHIN IMPLANT, SUBSEQUENTLY HAD DEVICE EXPLANTED 8 WEEKS POST-OPERATIVELY DUE TO DISPLACEMENT AND POOR WOUND HEALING.

  Patient problems: Failure of Implant; Impaired Healing

  MAUDE report 12598982 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K902824. One submission often covers many models, so check the product and lot details in each record.

• Z-2211-2013 · Aug 30, 2013 · Terminated
  Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M. To augment or reconstruct underdeveloped or traumatized mandibular region.