Vasoptic Medical’s Retinal Imaging Device Receives FDA 510(k) Clearance
The XyCAM retinal imaging device can allow ophthalmologists and optometrists to rapidly and affordably assess the vascular status of the retina, which can improve disease detection and treatment.
4WEB Medical Announces FDA 510(k) Clearance of Stand-Alone Anterior Lumbar Interbody Fusion Device
The new design allows fixation screws to be placed through the truss implant and into the adjacent vertebral bodies creating a zero-profile stand-alone construct that removes the need for supplemental fixation notes 4Web Medical.
Donald L Deyo Appointed Chairman and Head of US Operations at LindaCare
Donald L. Deyo is a medtech veteran with extensive experience in development and commercialization of cardiac disease therapies. In the new roles he will guide acceleration of growth in the US and strategic expansion into areas adjacent to and leveraging the Company's flagship OnePulse™ remote monitoring platform.
Ceek Women’s Health and Lupin Sign a Marketing Agreement
Under the promotional arrangement, Lupin's sales representatives will detail and demonstrate Ceek products including the Nella NuSpec (the Smarter Reusable Vaginal Speculum), VuSleeve, and VuLight products, alongside Lupin Women's Health flagship product, Solosec® (secnidazole) 2g oral granules indicated for the treatment of bacterial vaginosis (BV), a common vaginal infection in adult women.16.
GTX medical Granted FDA Breakthrough Device Designation for Go-2 Targeted Epidural Spinal Stimulation (TESS) System
The Go-2 System by GTX medical provides Targeted Epidural Spinal Stimulation therapy, promoting the recovery of leg motor functions and neurological control in adults with spinal cord injuries.