Israel-based Scopio Labs introduced the FDA granted De Novo clearance for its Full-Subject Bone Marrow Aspirate (FF-BMA) software program that gives AI-enabled determination assist instruments for bone marrow evaluation.
The FF-BMA software permits for bone marrow aspirate evaluation. It combines full-field imaging and an AI-powered determination assist system that enables hematopathologists to research bone marrow smears remotely.
Scopio Labs produces machines that course of blood and different cells in excessive element. The corporate sells an software that’s much like the newly cleared software referred to as Full-Subject Peripheral Blood Smear (FF-PBS) that’s primarily based on peripheral blood smears.
“Scopio’s full discipline bone marrow aspirate software addresses the pressing want for digital innovation amid the rising prevalence of hematologic situations and healthcare calls for,” Adam Bagg, professor of pathology and laboratory medication within the Perelman Faculty of Drugs on the College of Pennsylvania and lead investigator within the bone marrow aspirate examine, stated in an announcement.
“By optimizing digital workflows and enabling distinctive distant evaluate of total smears, we’re hopeful this expertise may help improve effectivity throughout the board.”
Salt Lake Metropolis-based AI-enabled mind well being firm Epitel acquired FDA 510(ok) clearance for 2 gadgets: REMI Distant Monitoring System for Ambulatory and REMI Vigilenz for Occasion Detection.
REMI Ambulatory permits for prolonged EEG recording to permit sufferers to be monitored whereas at-home and going about their every day lives. The software program, which makes use of the identical sensors as the corporate’s REMI for Healthcare Facility Use, permits sufferers and caregivers to mark when a affected person has a medical occasion or suspected occasion.
REMI Vigilenz AI for Occasion Detection is supposed to assist clinicians analyze EEG recordings obtained from the corporate’s REMI Distant EEG Monitoring System electroencephalogram (EEG). The software program makes no diagnostic conclusions, however is meant to help clinician’s skilled judgment.
“Current EEG monitoring techniques have been cumbersome and restrictive for sufferers, and technical necessities and limitations have impeded suppliers’ skill to manage, report, and interpret EEG. REMI Ambulatory and REMI Vigilenz AI For Occasion Detection will assist sufferers and suppliers make better-informed therapy selections,” Mark Lehmkuhle, CEO and cofounder of Epitel, stated in an announcement.
New Jersey-based digital girls’s well being firm Curio Digital Therapeutics acquired 510(ok) clearance for MamaLift Plus, a prescription digital therapeutic for the therapy of postpartum despair.
MamaLift Plus, obtainable via prescription solely, is meant to deal with sufferers 22 and over with gentle to reasonable postpartum despair utilizing neurobehavioral interventions that concentrate on addressing routine, maladaptive behaviors and dysfunctional ideas.
Neurobehavioral remedies embrace behavioral activation remedy, cognitive behavioral remedy, dialectical habits remedy and interpersonal remedy.
The providing is meant for use alongside outpatient care and is accessible on any smartphone or pill.
“Our aim has all the time been to offer progressive options for girls’s well being, particularly across the challenges they face with behavioral well being. MamaLift Plus is the primary and solely digital answer that may assist tackle the intense unmet want uniquely confronted by girls who’ve just lately delivered,” Shailja Dixit, CEO and founding father of Curio Digital Therapeutics, stated in an announcement.
