MAUDE Adverse Event Report: Treace Medical Concepts, Inc. Lapiplasty System 1; Plate

Model Number	SK12
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Skin Inflammation/ Irritation (4545)
Date of Event	09/03/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that after an initial bunion surgery on (b)(6) 2021, hardware was removed on (b)(6) 2026 due to hardware irritation.There were no deficiencies or malfunctions alleged/found with any tmc device and no other patient outcomes were reported as a result of this event.
Additional Manufacturer Narrative
It was reported that after an initial bunion surgery on (b)(6) 2021, hardware was removed on (b)(6) 2026 due to hardware irritation.There were no deficiencies or malfunctions alleged/found with any tmc device and no other patient outcomes were reported as a result of this event.No devices were returned for evaluation.The device history records were reviewed, and no issues were identified during the manufacture and release of the devices that could have contributed to what was reported.The most likely cause of the reported event could not be determined based on the available information and without the return of the device.The company will supplement the mdr as necessary and appropriate.An additional tmc device explanted in the same revision surgery was reported in 3011623994-2026-00256.

• Brand Name: Lapiplasty System 1
• Common Device Name: Plate
• Manufacturer (Section D): Treace Medical Concepts, Inc.; 100 palmetto park place; ponte vedra FL 32081
• Manufacturer (Section G): Treace Medical Concepts, Inc.; 100 palmetto park place; ponte vedra FL 32081
• Manufacturer Contact: artillia walker ; 100 palmetto park place; ponte vedra, FL 32081 ; +1(904)913-1020
• MDR Report Key: 50914283
• Report Number: 3011623994-2026-00255
• Device Sequence Number: 5344794
• Product Code: HRS
• UDI-Device Identifier: 00810111221337
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K251135
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2026
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 09/28/2026

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: 07/16/2022
• Device Model Number: SK12
• Device Lot Number: 19070013316
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/03/2026
• Initial Report FDA Received Date: 09/28/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 07/16/2019
• 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: 22 YR
• Patient Sex: Female