3i T3® BOET3210Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00844868033202), received between Dec 16, 2019 and Apr 28, 2022 — classified as 4 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 18, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryApr 28, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED IMPLANT REMOVED DUE TO INFECTION AND EXCESSIVE BONE LOSS.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 14237834 ↗
• InjuryApr 28, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT WAS REMOVED DUE TO INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 14237477 ↗
• InjuryJun 26, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT BOET3210 WAS REMOVED DUE TO LACK OF PRIMARY STABILITY THE SAME DAY IT WAS PLACED. PATIENT WILL GO BACK TO THE DENTAL PRACTICE TO PLACE ANOTHER IMPLANT OF LARGER DIAMETER.

  Patient problems: No Information

  MAUDE report 10199557 ↗
• InjuryDec 16, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED IMPLANT WAS REMOVED DUE TO INFECTION. ANOTHER IMPLANT WAS PLACED.

  Patient problems: Unspecified Infection

  MAUDE report 9471978 ↗