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    DIGITAL SURGERY SYSTEMS, INC

    FDA registration
    DIGITAL SURGERY SYSTEMS, INC·2 products·🇺🇸 United States

    RE3

    FDA UDI
    Digital Surgery Systems, Inc.·08600105136202·RE3 robotic excoscope system and accessories.

    IS2000 DAVINCI S SYSTEM

    FDA Adverse Event
    Other ·INTUITIVE SURGICAL,INC.·Product code NAY·May 22, 2013

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·July 15, 2025

    SMARTABLATE¿ SYSTEM RF GENERATOR (US)

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·December 5, 2019

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·June 5, 2023

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·September 25, 2022

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·June 6, 2023

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 3, 2016

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·February 18, 2020

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 11, 2025

    DA VINCI SP

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·June 17, 2025

    O-ARM 1000 IMAGING SYSTEM 3RD EDITION

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 30, 2016

    DAVINCI SI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 13, 2023

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·February 20, 2026

    CAIMAN DISP.INSTR.ARTICULAT.D5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·February 27, 2017

    DA VINCI X

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·February 18, 2026

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·December 27, 2016

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·December 16, 2025

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·August 26, 2025