3i T3® DCD® BNSS310Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00844868028970), received between Nov 14, 2022 and Jun 29, 2023 — classified as 2 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 29, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT COMPLAINED OF PAIN AND SWELLING. THE IMPLANT WAS REMOVED DUE TO PERI-IMPLANTITIS. OTHER SYMPTOMS: ABSCESS AND INFLAMMATION.

  Patient problems: Osteolysis; Stomatitis; Unspecified Infection

  MAUDE report 17224943 ↗
• InjuryNov 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT DURING A 2ND STAGE PROCEDURE, THE IMPLANT AT TOOTH LOCATION #20 WAS FOUND TO HAVE BONE LOSS ON THE BUCCAL AND MESIAL DESPITE BEING STABLE. THE IMPLANT WAS REMOVED TO PREVENT FURTHER BONE LOSS.

  Patient problems: Osteolysis

  MAUDE report 15790160 ↗