MAUDE Adverse Event Report: INSTITUT STRAUMANN AG TLC SP Ø5.5MM WT, SLACTIVE® 6MM RXD; ENDOSSEOUS DENTAL IMPLANT

Catalog Number	035.7706S
Medical Device Problem Code	Failure to Osseointegrate (1863)
Health Effect - Clinical Codes	Unspecified Infection (1930); Fibrosis (3167); Hyperresponsive to stimuli (4538)
Date of Event	12/19/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
The clinician reports the implant was inserted (b)(6) 2025 in ada 3.Details of surgery: implant surface not completely covered with bone.On (b)(6) 2025, non-osseointegration was verified.Patient presented with previous bone augmentation.The device was forwarded to the manufacturer.At the event the patient experienced: peri-implantitis, mobility and increased sensitivity.No further patient complications were reported.

• Brand Name: TLC SP Ø5.5MM WT, SLACTIVE® 6MM RXD
• Common Device Name: ENDOSSEOUS DENTAL IMPLANT
• Manufacturer (Section D): INSTITUT STRAUMANN AG; peter merian-weg 12; basel 04002 ; SZ 04002
• MDR Report Key: 24236557
• Report Number: 0001222315-2026-000293
• Device Sequence Number: 10187723
• Product Code: DZE
• UDI-Device Identifier: 07630031766168
• UDI-Public: 07630031766168
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• Device Explanted Year: 2025
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date (Section B): 02/02/2026
• Report Date (Section F): 01/07/2026

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: 035.7706S
• Device Lot Number: CPTH6
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/07/2026
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 02/02/2026
• Device Age: 21 MO
• Event Location: Other
• Date Report to Manufacturer: 01/07/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 02/02/2026
• 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: 58 YR
• Patient Sex: Male