Clinical Research Directory

Inclusion Criteria: * Subject is at least 18 years old. * Subjects able to provide written informed consent. * Subject deemed eligible candidate by surgeon and will comply with the study procedures. * Subjects with ventral hernia. * Subjects with ASA grade I to III. * Subject must sign and date informed consent prior to treatment. * Subject can undergo general anesthesia per anesthesiologist assessment. Exclusion Criteria: * Women who are pregnant or breast-feeding or who wish to become pregnant during the period of the clinical investigation. * Subject has medical condition, which in the judgement of the investigator makes the subject a poor candidate for the investigational procedure. * Participation in another clinical trial that is in the active phase. * Subject unwilling or inability to follow procedures outlined in the protocol. * Subjects who are not suitable for robotic surgery, the Subject will be excluded from the study and the will be considered a screen failure and the surgeon will proceed with a standard multiport laparoscopic Hernia repair. * Subjects who present any adverse event before use the Anovo Surgical System ("Anovo") that can affect evaluation of safety and performance of Investigational Device.