Da Vinci Services
Optimize your robotic-assisted surgery program
Experienced technical guidance
Keep your robotics-assisted surgery program running smoothly. Access a pool of Intuitive technical engineers with an average of 10+ years1 of hands-on system experience.
- Technical support
- Service engineer network
- Ordering and customer hotline
- Training support
Develop strengths within your da Vinci program
- CSSD/SPD support
- Genesis program
- Market access and custom analytics
The Intuitive Ecosystem
The Intuitive Ecosystem
Designed to support hospitals throughout their minimally invasive care journey, this integrated ecosystem brings together advanced technology, professional education, and program optimization resources. Built around the da Vinci and Ion platforms, it creates a connected experience that helps care teams achieve their goals, maximize program value, and continuously optimize patient care.
Access Intuitive system data when you need it
Learn our best practices for reprocessing
Operational data and workflows in your hands
Proactive services powered by OnSite
- As of Q1 2025. Internal data on file.
Disclosures
Da Vinci X & Xi Surgical Systems
The Intuitive Surgical Endoscopic Instrument Control Systems (da Vinci X and da Vinci Xi Surgical Systems) are intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments during urologic surgical procedures, general laparoscopic surgical procedures, gynecologic laparoscopic surgical procedures, general thoracoscopic surgical procedures, and trans-oral otolaryngology surgical procedures restricted to benign tumors and malignant tumors classified as T1 and T2, and for benign base of tongue resection procedures. The systems are indicated for adult and pediatric use (except for trans-oral otolaryngology surgical procedures). They are intended to be used by trained physicians in an operating room environment.
The da Vinci X and da Vinci Xi Surgical Systems are class IIb medical devices CE marked (CE 2460) under the European Medical Devices Regulation (EU 2017/745), manufactured by Intuitive Surgical, Inc. Refer to Instructions For Use before use.
Da Vinci 5 Surgical System
The da Vinci 5 Surgical System is intended to assist in the accurate control of da Vinci endoscopes and instruments during minimally invasive endoscopic urologic surgical procedures, gynecologic surgical procedures, general laparoscopic surgical procedures and thoracoscopic surgical procedures. The system is indicated for adult and pediatric use. It is intended to be used by trained physicians in an operating room environment.
The da Vinci 5 Surgical System is a class IIb medical device CE marked (CE 2460) under the European Medical Devices Regulation (EU 2017/745), manufactured by Intuitive Surgical, Inc. Refer to Instructions For Use before use.
Da Vinci SP Surgical System
The da Vinci SP Surgical System is intended to assist in the accurate control of the da Vinci SP endoscope and instruments during minimally invasive endoscopic abdominopelvic, thoracoscopic, transoral otolaryngology, transanal colorectal, and breast surgical procedures. The system is indicated for adult use. It is intended to be used by trained physicians in an operating room environment.
The da Vinci SP Surgical System is a class IIb medical device CE marked (CE 2460) under the European Medical Devices Regulation (EU 2017/745), manufactured by Intuitive Surgical, Inc. Refer to Instructions For Use before use.
Ion Endoluminal System
The Ion Endoluminal System assists the user in navigating a catheter and endoscopic tools in the pulmonary tract using endoscopic visualization of the tracheobronchial tree for diagnostic and therapeutic procedures. The Ion Endoluminal System enables fiducial marker placement. It does not make a diagnosis and is not for pediatric use.
The Flexision Biopsy Needle is used with the Ion Endoluminal System to biopsy tissue from a target area in the lung.
The PlanPoint Software uses patient CT scans to create a 3D plan of the lung and navigation pathways for use with the Ion Endoluminal System.
The Ion Endoluminal System, the Flexision Biopsy Needle and the PlanPoint Software are class IIa medical devices CE marked (CE 2460) under the European Medical Devices Regulation (EU 2017/745), manufactured by Intuitive Surgical, Inc. Refer to Instructions For Use before use.
Intuitive technology should only be used by physicians and staff who have received specific training in the use of Intuitive technology. Training provided by Intuitive is limited to the use of Intuitive technology, instruments, and accessories. It does not replace the necessary medical training and experience required to perform surgical procedures. Nothing in Intuitive’s training curricula makes expressed or implied promises or commitments to the persons attending. Some of the training described in Intuitive promotions may be provided by organizations or entities other than Intuitive.
Legal Notices
Individuals' outcomes may depend on a number of factors, including but not limited to patient characteristics, disease characteristics and/or physician/surgeon experience.
Some products, features or technologies may not be available in all countries. Please contact your local Intuitive representative for product availability in your region. Refer to the product specific User Manual for indications, contraindications, warnings and other product information.