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.