Momentis Surgical wins FDA clearance for its surgical robot
October 15, 2024
Momentis Surgical (formerly Memic) announced today that it received FDA 510(k) clearance for its Anovo robotic surgical platform.
Momentis Surgical (formerly Memic) announced today that it received FDA 510(k) clearance for its Anovo robotic surgical platform.
CMR Surgical announced today that it received FDA de novo clearance to market its Versius surgical robot platform.
Regenity Biosciences announced that it received FDA 510(k) clearance for its RejuvaKnee implant for soft tissue injuries of the meniscus.
Procept BioRobotics (Nasdaq:PRCT) announced today that the FDA approved an investigational device exemption (IDE) trial for its Aquablation therapy.
Corin announced that it received FDA 510(k) clearance for its Unity Knee medial constrained (MC) tibial insert.
Zeiss Medical Technology announced today that it launched the Kinevo 900 S robotic visualization system for neurosurgery procedures.
Alesi Surgical has received FDA 510(k) clearance of its Ultravision2 IonPencil for cutting and coagulating soft tissue in open surgery while managing surgical smoke.
It is the first magnetically controlled prosthetic hand that allows amputees to reproduce all movements simply by thinking and to control the force applied when grasping fragile objects. No wires, no electrical connection, only magnets and muscles to control the movements of the fingers and enable everyday activities such as opening a jar, using a screwdriver, picking up a coin.
FREMONT, Calif., Sept. 10, 2024 /PRNewswire/ — THINK Surgical, Inc., an innovator in the field of orthopedic surgical robots, today announced the successful completion of the first total knee arthroplasty procedure utilizing its new TMINI® Miniature Robotic System version 1.1 following recent FDA 510(k) clearance.
FREMONT, Calif., Sept. 5, 2024 /PRNewswire/ — THINK Surgical, Inc., an innovator in the field of orthopedic surgical robots, today announced that its TMINI® Miniature Robotic System has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for use with the Persona® The Personalized Knee System® from Zimmer Biomet.