MAUDE Adverse Event Report: Institut Straumann AG BLX ?6.5 WB, SLA? 10mm, RXD; Endosseous Dental Implant

Catalog Number	061.9510
Medical Device Problem Code	Loss of Osseointegration (2408)
Health Effect - Clinical Codes	Fibrosis (3167); Hyperresponsive to stimuli (4538)
Date of Event	05/28/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
The clinician reports the implant was inserted (b)(6) 2025 in ada 15.Details of surgery: immediate extraction site.On (b)(6) 2026 loss of osseointegration was verified.The device was forwarded to the manufacturer.At the event the patient experienced: mobility and increased sensitivity.No further patient complications were reported.

• Brand Name: BLX ?6.5 WB, SLA? 10mm, RXD
• Common Device Name: Endosseous Dental Implant
• Manufacturer (Section D): Institut Straumann AG; peter merian-weg 12; basel 04002 ; SZ 04002
• MDR Report Key: 50022782
• Report Number: 0001222315-2026-002222
• Device Sequence Number: 13177255
• Product Code: DZE
• UDI-Device Identifier: 07630031743916
• UDI-Public: 07630031743916
• Combination Product (Y/N): N
• Initial Reporter State: ID
• Initial Reporter Country: US
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• 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): 07/24/2026
• Report Date (Section F): 07/24/2026

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 Catalogue Number: 061.9510
• Device Lot Number: LJGK1
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 06/30/2026
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 07/24/2026
• Device Age: 14 MO
• Event Location: Other
• Date Report to Manufacturer: 06/30/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 07/27/2026
• 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 Age: 79 YR
• Patient Sex: Male