Philips’ new X11-4t Mini 3D TEE ultrasound transducer has received US FDA approval.
Medtronic has received the CE Mark for its Micra AV2 and Micra VR2 miniature, leadless pacemakers.
Medtronic has received CE Mark approval for their MiniMed 780G system with Simplera Sync, a disposable, all-in-one continuous glucose monitor (CGM) requiring no fingersticks or overtape. Simplera Sync features an improved user experience with a simple, two-step insertion process and is half the size of previous Medtronic sensors.
Stryker has expanded its Gamma4 Hip Fracture Nailing System, with the addition of an intermediate nail, the RC Lag Screw, and an anti-rotation clip with sleeve components. Since its launch in August of 2022, the Gamma4 System has been used in over 19,000 cases across more than 850 facilities, solidifying its position as a leading […]
Innovia Medical showcased their DTR Medical Cervical Rotating Biopsy Punch at this year’s Arab Health Exhibition in Dubai. The device is designed for obtaining cervical biopsies during gynaecological procedures. The device’s single-use eliminates cross-contamination.
Marking a pivotal point in a nine-year journey of innovation, OTSAW, a leader in Singapore’s robotics landscape, introduces Camello+, an autonomous mobile robot (AMR) poised to revolutionize various industries, including healthcare.
Medtronic has received US FDA approval for the PulseSelect Pulsed Field Ablation (PFA) System for the treatment of both paroxysmal and persistent atrial fibrillation (AF). This is the first PFA technology to receive FDA approval and follows the European CE Mark approval for the PulseSelect PFA system in November.
Shanghai CMD Medical has introduced the SFD, a suction/irrigation attachment device, which revolutionizes ear endoscopy surgery with its patented design. This breakthrough innovation combines suction and irrigation functionalities within the ear endoscope. By reducing the need for a separate device to perform such procedures, surgeons are now able to perform most surgeries without assistance, enhancing […]
JUNE Medical’s Galaxy II self-retaining surgical retractor has received Medical Device Regulation (MDR – Regulation (EU) 2017/745) certification from BSI Group for its use in the European Union. This accreditation is testament to the value that this innovative selfretaining retractor brings to improving patient safety and the overall quality of healthcare across all surgical specialties.
InfoBionic, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for MoMe ARC, their 3rd Generation remote ECG monitoring device paired with their inaugural Bluetooth diagnostic 6-lead sensor designed to aid physicians in their diagnosis of cardiac arrhythmias in patients with a demonstrated need for cardiac monitoring.
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