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US-based organ transplant company Paragonix Technologies has received the US Food and Drug Administration (FDA) approval for BAROguard, its next-gen donor lung preservation system. BAROguard is designed to
Stimlabs LLC, (“StimLabs”), a leader in regenerative medicine, announced the launch of Relese, a fenestrated dehydrated complete human placental membrane (dCHPM) allograft for chronic and acute wounds. As the
US-based medical equipment manufacturer Sanuwave Health has agreed to merge with SEP Acquisition (SEPA), a special purpose acquisition company (SPAC), to become a publicly listed company. SEPA is
US-based non-invasive monitoring technologies provider Masimo has announced the full commercial release of its Stork smart home baby monitoring system in the US. The Stork system leverages Masimo’s
The heart teams at the Piedmont Heart Institute in Atlanta, Georgia, USA and the University of Virginia Health System in Charlottesville, VA, USA, successfully performed the first two implantations in the US
US-based medical technology company Levita Magnetics has received the US Food and Drug Administration (FDA) approval for its MARS platform. The Levita MARS system is a minimally invasive
Convergent Genomics announced that its non-invasive genomic urine test UroAmp can detect bladder cancer and predict its recurrence before the onset of symptoms, based on data from a
Regenesis Biomedical, Inc., a medical device company focused on safe, non-drug, pain management, announced today commercialization of the new Reprieve by Regenesis™ device (Reprieve). Reprieve is the only
US-based medical device company Exactech has received the US Food and Drug Administration (FDA) 510(k) approval for a new Activit-E polyethylene, used with its Truliant knee replacement system.
Israeli medical device startup Nurami Medical has received the US Food and Drug Administration (FDA) 510(k) approval for its electrospun nanofiber-based product, ArtiFascia Dura Substitute. ArtiFascia is a