3i T3® DCD® BNST610Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00844868029342), received between Dec 10, 2021 and Mar 7, 2025 — classified as 3 injuries.

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 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMar 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE DOCTOR REPORTS THAT THE DENTAL IMPLANT LOCATED IN DENTAL POSITION NUMBER #26 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS IN THE PER THAT THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANT.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 21544935 ↗
• InjuryJun 12, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT WAS PLACED A FEW YEARS BEFORE RESTORING THE IMPLANT. UPON REQUEST OF RESTORATION, A RADIOGRAPH WAS TAKEN WHICH NOTED BONE LOSS AROUND THE IMPLANT. THE IMPLANT WAS REMOVED. SYMPTOMS AS A RESULT OF THE EVENT: INFECTION AND PAIN.

  Patient problems: Osteolysis; Pain; Unspecified Infection

  MAUDE report 17106719 ↗
• InjuryDec 10, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT LOST INTEGRATION DUE TO PERI-IMPLANTITIS AT THE IMPLANT SITE AND WAS REMOVED BECAUSE OF SEVERE INFECTION, BONE LOSS AND DRAINING.

  Patient problems: Abscess; Osteolysis; Pain; Unspecified Infection

  MAUDE report 12975313 ↗