VACS Device Clinical Study for Incontinence Treatment: Follow up Study

Inclusion Criteria: * Patients who participated in the study titled "Clinical Evaluation of Vaginal Suture Knotting Device in the Treatment of Urinary Incontinence in Women" (protocol code VACS-D) and completed their final follow-up visit (the 6-12-month visit). * Volunteers who are willing to participate, have been informed about the study, and have provided a signed informed consent form (ICF), stating that they can comply with the requirements and restrictions listed in the ICF and this protocol. Exclusion Criteria: * Having received radiotherapy during the postoperative period as part of the VACS-D study. * Women who are pregnant based on the results of a urine pregnancy test. * Those who have been enrolled in any other clinical trial following the VACS-D protocol study.