FDA clears first stapler for single-port robotics from Intuitive
April 10, 2025
Intuitive (Nasdaq: ISRG) announced today that it received FDA clearance for its fully wristed SP SureForm 45 stapler.
Intuitive (Nasdaq: ISRG) announced today that it received FDA clearance for its fully wristed SP SureForm 45 stapler.
Zeiss Medical Technology announced today that it received FDA 510(k) clearance for the Intrabeam 700 platform.
The latest advance in wearable robotic technology promises to solve a 200-year-old problem by revolutionizing the fit of prosthetic limbs, transforming the lives of millions of amputees worldwide.
Monogram Technologies secured 510(k) clearance for its robotic knee replacement system
Moon Surgical announced today that it received FDA clearance for ScoPilot, a Nvidia-enabled platform for its Maestro surgical robot.
Lifeward (Nasdaq:LFWD) announced today that it received FDA 510(k) clearance for its latest-generation personal exoskeleton device, ReWalk 7.
Spineart and eCential Robotics today announced the receipt of FDA 510(k) clearance for the use of an application for robotic navigation.
Using Nvidia and GE Healthcare technology, the robotic surgery system is intended to help doctors detect lung cancer earlier.
Johnson & Johnson MedTech (NYSE: JNJ)+
announced today that the FDA cleared its Monarch Quest technology for robotic-assisted bronchoscopy.
Spinal cord injuries are life-altering, often leaving individuals with severe mobility impairments. While rehabilitation robotics—devices that guide movement during therapy—have improved training for those with spinal cord injuries, their effectiveness remains limited. Without active muscle engagement, robotic-assisted movement alone does not sufficiently retrain the nervous system.