Medtronic Enhances AiBLE Ecosystem for Spinal Procedures
Medtronic launched new software, hardware, and imaging innovations for its AiBLE ecosystem, aimed at improving spine and cranial surgeries.
Medtronic launched new software, hardware, and imaging innovations for its AiBLE ecosystem, aimed at improving spine and cranial surgeries.
InnoVoyce has received FDA 510(k) clearance for the VYLO Laser System, a 455nm blue light laser offering up to 30 watts of power.
Olympus is recalling its Olympus High Flow Insufflation Unit because the unit may over-insufflate (inflate) air into the body with no warning.
Medtronic launched new software, hardware, and imaging innovations for its AiBLE ecosystem, aimed at improving spine and cranial surgeries.
BD’s sale of its Surgical Implementation platform to STERIS will include V. Mueller, Snowden-Pencer, and Genesis branded products and three manufacturing facilities.
Read MoreNova Eye Medical Limited has been granted U.S. FDA 510(k) clearance for its new canaloplasty device, iTrackAdvance.
Read MoreProximie commenced the rollout of a smart glasses solution for use in operating rooms, following its initial introduction earlier this year.
Read MoreAsensus Surgical received FDA 510(k) clearance for an expanded indication to treat pediatric patients with the Senhance Surgical System.
Read MoreLydus Medical received FDA clearance 510(k) for a microvascular anastomosis suture deployment system for standardized omni-vessel anastomoses.
Read MoreSURGLASSES announced that its Caduceus S AR Spine Navigation System has received 510(k) clearance from the U.S. FDA.
Read MoreMediView XR has engaged with Mayo Clinic to explore ways to advance procedural augmented reality solutions.