Registry/Surgical robots
Surgical robots
Robotic systems for surgical procedures: assistive, semi-autonomous, and increasingly autonomous platforms.
Surgical robotics span teleoperated platforms (Intuitive da Vinci as the canonical case), semi-autonomous orthopedic systems (Stryker Mako, Smith+Nephew CORI), and emerging autonomous-anastomosis research platforms. Operating under FDA 510(k) and PMA regulation; deployment count reads commercial procedure volume rather than installed-unit count. Coverage on DEPLOY tracks the verified product surface and the regulatory clearance state for each manufacturer.
Companies (15)
View all →- Asensus Surgical
Durham, North Carolina, USA
- Brain Navi
Zhubei, Taiwan
- Brainlab
Munich, Germany
- CMR Surgical
Cambridge, United Kingdom
- Distalmotion
Lausanne, Switzerland
- Intuitive Surgical
Sunnyvale, California, USA
- Johnson & Johnson
New Brunswick, New Jersey, USA
- Medtronic
Dublin, Ireland
- Monogram Technologies
Austin, Texas, USA
- Moon Surgical
San Carlos, California, USA
- Smith+Nephew
United Kingdom
- Stereotaxis
St. Louis, Missouri, USA
Models (16)
Intuitive (da Vinci)(2)
- da Vinci (and Ion)by Intuitive Surgicalproduction
- Ion Endoluminal Systemby Intuitive Surgicalcommercial
Zimmer Biomet (ROSA)(1)
- ROSAby Zimmer Biometcommercial
Asensus (Senhance)(1)
- Senhanceby Asensus Surgicalcommercial
Monogram(1)
- mBos TKA Systemby Monogram Technologiesresearch
Emerging(9)
- Cirqby Brainlabcommercial
- CORIby Smith+Nephewcommercial
- Dexterby Distalmotioncommercial
- Genesis RMN / GenesisXby Stereotaxiscommercial
- Maestroby Moon Surgicalcommercial
- NaoTracby Brain Navicommercial
- Versiusby CMR Surgicalcommercial
- Ottavaby Johnson & Johnsonresearch
- V1by Vicarious Surgicalresearch
Regulations (1)
- EU Artificial Intelligence Act (Regulation (EU) 2024/1689)European Union · other
Incidents (13)
View all →- da Vinci 8mm SureForm 30 Gray stapler reload recall after incomplete staple lines (1 death, 4 serious injuries)recall · 2026-03-11
- da Vinci X/Xi/5 recall: software error let instrument arms failing a ball-screw diagnostic stay in userecall · 2026-02-02
- Intuitive Ion Endoluminal System recall: probe-bag sterile-seal issue (Z-1134-2026)recall · 2026-01-28
- da Vinci 5 console foot-pedal recall over a spring failure that can leave a pedal stuck pressedrecall · 2025-02-26
- Intuitive Ion Endoluminal System recall: instrument-cart-arm screw issue (Z-2720-2024)recall · 2024-09-04
- Stryker Mako Total Knee software correction over 'error #3' codes when switching applicationsrecall · 2024-05-28
- Asensus Senhance Class I recall: software malfunction caused uncontrolled arm motion after disengaging teleoprecall · 2023-09-15
- da Vinci X/Xi recall: loose instrument carriage from an out-of-spec linear-rail componentrecall · 2023-02-23
- da Vinci Xi 8mm SureForm 30 stapler recall over staple-deployment failure and device fragmentsrecall · 2022-10-07
- Zimmer Biomet ROSA ONE Brain 3.1 Class I recall: software could drive instruments to a wrong trajectoryrecall · 2021-09-22
- Intuitive Ion Endoluminal System recalls (fully-articulating catheter and Flexison biopsy needle)recall · 2020-12-02
- FDA warning letter to Intuitive Surgical over late reporting of da Vinci corrections and adverse eventsregulatory_action · 2013-07-19
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