MAUDE Adverse Event Report: ALMA LASERS LTD. HYBRID SYSTEM 70W 120V 50/60 HZ; POWERED LASER SURGICAL INSTRUMENT

Model Number	1
Medical Device Problem Code	Use of Incorrect Control/Treatment Settings (1126)
Health Effect - Clinical Code	Burn(s) (1757)
Date of Event	10/30/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
Following use of the hybrid system at a user facility, a patient experienced a burn at the treatment site.Investigation by alma lasers inc.Found that the burn will likely leave a permanent scar.

• Brand Name: HYBRID SYSTEM 70W 120V 50/60 HZ
• Common Device Name: POWERED LASER SURGICAL INSTRUMENT
• Manufacturer (Section D): ALMA LASERS LTD.; 18 haharash street; north industrial park; caesarea, 30798 95; IS 3079895
• MDR Report Key: 23752605
• Report Number: 3004450661-2025-00025
• Device Sequence Number: 13157633
• Product Code: GEX
• UDI-Device Identifier: 17290110122109
• UDI-Public: 17290110122109
• Combination Product (Y/N): N
• Initial Reporter State: HI
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Nurse Practitioner
• Type of Report: Initial
• Report Date (Section B): 12/08/2025
• Report Date (Section F): 12/08/2025

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 Model Number: 1
• Device Catalogue Number: AACO15061980BDAZ0003
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: Yes
• Device Age: 5 MO
• Event Location: Outpatient Treatment Facility
• Date Report to Manufacturer: 11/14/2025
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 12/08/2025
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 66 YR
• Patient Sex: Female
• Date Report Sent to FDA: 12/08/2025