Corin wins FDA nod for Unity Knee tibial insert for robot-assisted TKA
October 4, 2024
Corin announced that it received FDA 510(k) clearance for its Unity Knee medial constrained (MC) tibial insert.
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.
Vitestro says it is the first company ever to achieve CE marking for an autonomous blood drawing device.
Think Surgical announced that the FDA granted 510(k) clearance for its TMINI miniature robotic system for use with Medacta’s knee systems.
SUNRISE, Fla., Aug. 26, 2024 /PRNewswire/ — Obvius Robotics, a medical device company developing an innovative technology platform for democratizing vascular access, today announced the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device Designation for its CERTA Access System for central venous catheterization (CVC).
RENO, Nev. and ROCKVILLE, Md., Aug. 23, 2024 /PRNewswire/ — Melzi Surgical, a medical device company focused on providing innovative technology to locate lost surgical sharps and Spartan Medical Inc., a veteran-owned medical solutions company, have launched a campaign to raise awareness around the impacts of Retained Surgical Items (RSIs) and near-misses to provide a unique offering to reduce RSIs and potential consequences.