MAUDE Adverse Event Report: Institut Straumann AG BL, ? 3.3 mm NC, SLActive 10 mm; Endosseous Dental Implant

Catalog Number	021.2110
Medical Device Problem Code	Loss of Osseointegration (2408)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	08/11/2026
Type of Reportable Event	Serious Injury

• Brand Name: BL, ? 3.3 mm NC, SLActive 10 mm
• Common Device Name: Endosseous Dental Implant
• Manufacturer (Section D): Institut Straumann AG; peter merian-weg 12; basel 04002 ; SZ 04002
• MDR Report Key: 50824455
• Report Number: 0001222315-2026-002882
• Device Sequence Number: 10218381
• Product Code: DZE
• UDI-Device Identifier: 07630031706355
• UDI-Public: 07630031706355
• Combination Product (Y/N): N
• Initial Reporter State: IN
• Initial Reporter Country: US
• Summary Report (Y/N): N
• Device Implanted Year: 2012
• Device Explanted Year: 2026
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date (Section B): 09/18/2026
• Report Date (Section F): 09/18/2026

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: 08/31/2017
• Device Catalogue Number: 021.2110
• Device Lot Number: ET449
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 08/25/2026
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 09/18/2026
• Device Age: 168 MO
• Event Location: Other
• Date Report to Manufacturer: 08/25/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 09/18/2026
• 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 Sex: Male