MAUDE Adverse Event Report: APPLIED MEDICAL RESOURCES STEALTH® CLAMPS; CLAMP, VASCULAR

Model Number	A3203
Medical Device Problem Codes	Failure to Align (2522); Patient Device Interaction Problem (4001)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The event unit is anticipated to return to applied medical for evaluation.A follow-up report will be sent upon competition of investigation.
Event or Problem Description
Procedure performed: urological procedure on the spermatic cord.Event description: the stealth clamp was used regularly for a urological procedure on the spermatic cord.Reason: tear due to frequent use.Parallel clamping no longer possible due to frequent use.Additional information received by applied medical rep via email on 11aug25: the surgeon describes it colloquially as looking like "finger crossing" of the jaws.It was noticed before use.Patient status: no clinical impact to the patient.Intervention: user used his second a3203 stealth clamp.
Additional Manufacturer Narrative
The event unit was not returned to applied medical for evaluation.As the event unit was not returned, applied medical is unable to determine if the event unit exhibited any non-conformances that could have contributed to the reported event.In the absence of the event unit, it is difficult to determine if the reported event was caused by a manufacturing non-conformance or circumstantial factors at the time of use.Applied medical has reviewed the details surrounding the event and is unable to determine the exact root cause of the event.Applied medical has performed a historical trend analysis and review of production records and no relevant documentation was identified.Correction: e2 and h6, correcting health professional and device code information.
Event or Problem Description
Procedure performed: urological procedure on the spermatic cord.Event description: the stealth clamp was used regularly for a urological procedure on the spermatic cord.Reason: tear due to frequent use.Parallel clamping no longer possible due to frequent use.Additional information received by applied medical rep via email on 11aug25: the surgeon describes it colloquially as looking like ¿finger crossing¿ of the jaws.It was noticed before use.Patient status: no clinical impact to the patient.Intervention: user used his second a3203 stealth clamp.

• Brand Name: STEALTH® CLAMPS
• Common Device Name: CLAMP, VASCULAR
• Manufacturer (Section D): APPLIED MEDICAL RESOURCES; 22872 avenida empresa; rancho santa margarita CA 92688
• Manufacturer Contact: ashleigh mendez ; 22872 avenida empresa; rancho santa margarita, CA 92688 ; 9497135359
• MDR Report Key: 22841566
• Report Number: 2027111-2025-00703
• Device Sequence Number: 14684081
• Product Code: DXC
• UDI-Device Identifier: 00607915112721
• UDI-Public: (01)00607915112721
• Combination Product (Y/N): N
• Initial Reporter Country: GM
• PMA/510(K) Number: K950492
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 05/21/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: A3203
• Device Catalogue Number: 100497301
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/31/2025
• Supplement Date Received by Manufacturer: Not provided; Not provided
• Initial Report FDA Received Date: 08/19/2025
• Supplement Report FDA Received Date: 11/17/2025; 05/21/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown