3i T3® SHORT DCD® BNES605Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00844868033615), received between Jan 14, 2020 and Nov 18, 2024 — classified as 5 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryNov 18, 2024Adverse 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 #21 FAILED DUE TO PERI-IMPLANTITIS. THE DOCTOR REPORTS THAT THE PROCEDURE WAS NOT CONCLUDED BY PLACING ANOTHER IMPLANT. BONE TYPE: II. THE DOCTOR REPORTED PAIN AND ABSCESS.

  Patient problems: Osteolysis; Pain; Unspecified Infection

  MAUDE report 20703666 ↗
• InjuryJan 12, 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 PERI-IMPLANTITIS. THERE WAS POOR CROWN/ROOT RATIO. TOOTH #3.

  Patient problems: Osteolysis; Unspecified Infection

  MAUDE report 13236654 ↗
• InjurySep 7, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED IMPLANT REMOVED DUE TO PERI-IMPLANTITIS.SITE PRESENTED BONE LOSS, EDEMA, INFLAMMATION. PATIENT ALSO HAD PAIN. IMPLANT WAS LOADED WITH A METAL-CERAMIC BRIDGE.

  Patient problems: Edema; Inflammation; No Information; Pain; Unspecified Infection

  MAUDE report 10498794 ↗
• InjuryJan 17, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANT COULD NOT ACHIEVE PRIMARY STABILITY. THE IMPLANT WAS REMOVED AND NO OTHER IMPLANT WAS ABLE TO BE PLACED.

  Patient problems: No Information

  MAUDE report 9601366 ↗
• InjuryJan 14, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT AN IMPLANT (BNES605) WAS UNABLE TO BE PLACED INTO OSTEOTOMY. IMPLANT DID NOT ACHIEVE PRIMARY STABILITY AND IT WAS REMOVED. TOOTH LOCATION 3.

  Patient problems: No Information

  MAUDE report 9587116 ↗