MAUDE Adverse Event Report: INSTITUT STRAUMANN AG TE-IMPLANT, Ø4.1MM, WN, SLACTIVE, 10.0MM; ENDOSSEOUS DENTAL IMPLANT

Catalog Number	80494S
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/05/2023
Type of Reportable Event	Serious Injury
Event or Problem Description
The clinician reports that the day the implant was placed in ada 18, failure occurred upon insertion.Details of surgery: primary stability not achieved.The device was forwarded to the manufacturer.There were no reported patient injuries or complications.

• Brand Name: TE-IMPLANT, Ø4.1MM, WN, SLACTIVE, 10.0MM
• Common Device Name: ENDOSSEOUS DENTAL IMPLANT
• Manufacturer (Section D): INSTITUT STRAUMANN AG; peter merian-weg 12; basel 04002 ; SZ 04002
• MDR Report Key: 18511410
• Report Number: 0001222315-2024-001201
• Device Sequence Number: 14359863
• Product Code: DZE
• UDI-Device Identifier: 07630031727589
• UDI-Public: 07630031727589
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2023
• Device Explanted Year: 2023
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date (Section B): 01/15/2024
• Report Date (Section F): 12/21/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 03/12/2025
• Device Catalogue Number: 80494S
• Device Lot Number: ALA88
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 12/21/2023
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 01/15/2024
• Device Age: 45 MO
• Event Location: Other
• Date Report to Manufacturer: 12/21/2023
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 01/15/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 67 YR
• Patient Sex: Male