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Nevro unveils HFX Connect in Europe, gets expanded CE mark for HFX SCS system
US-based medical device company Nevro has launched HFX Connect in Europe and received the CE marking of expanded labelling for…
ZimVie receives expanded FDA approval for new Mobi-C implant
US-based ZimVie has received the US Food and Drug Administration (FDA) approval for a smaller height of the Mobi-C Cervical…
EPIC Health Launches New Remote Patient Monitoring Program in Collaboration with OMRON Healthcare to Address Health Inequities with VitalSight
EPIC Health, Detroit’s health system committed to community-focused healthcare, and OMRON Healthcare, a global heart health leader, today announced a…
Acorai receives Breakthrough Device Designation for their non-invasive intracardiac pressure monitor
Acorai, a start-up medical device manufacturer from Sweden, today announces that the U.S. Food and Drug Administration (FDA) has granted Breakthrough…
ReWalk Robotics to acquire Anti-Gravity systems provider AlterG for $19m
Medical device company ReWalk Robotics has agreed to acquire AlterG, a US-based provider of mobility enhancement products for physical therapy…
Theranica gets expanded CE mark indication for Nerivio in migraine
Theranica has secured expanded Conformité Européenne (CE) mark approval for Nerivio as dual-use therapy for acute and preventive treatment of…
Dentognostics Receives Significant Investment as It Seeks to Improve Patient Outcomes Against Periodontal Disease
Dentognostics, a research-driven technology company, has secured significant investments from Dental Innovation Alliance (DIA) and Dental365, further propelling its growth…
Fresenius Medical Care Partners with Sarah Bush Lincoln to Provide Life-Sustaining Care to Rural Patients
Fresenius Medical Care, the world’s leading provider of products and services for individuals with renal diseases has launched an on-site dialysis…
Orchestra BioMed secures FDA IDE approval for study of Virtue SAB
Biomedical company Orchestra BioMed has secured investigational device exemption (IDE) approval from the US Food and Drug Administration (FDA) for…
PENTAX gets FDA nod for PENTAX Medical INSPIRA and i20c endoscope series
HOYA Group’s unit PENTAX Medical America has received the 510(k) clearance from the US Food and Drug Administration (FDA) for…