CroíValve, an Irish-U.S. based medical device company with a novel, transcatheter solution for tricuspid regurgitation (TR), today announced initiation of its Early Feasibility Study...
SnoreLessNow announced today that the FDA granted 510(k) clearance for its over-the-counter dental device.
Known as SomniFit-S in Europe, the Anti-Snore Mouth Guard+ reduces snoring...
Pi-Cardia announced today that the FDA granted breakthrough device designation for its ShortCut leaflet modification device.
ShortCut facilitates valve-in-valve transcatheter aortic valve replacement (TAVR) procedures...
US-based insulin delivery technology company Modular Medical has submitted its next-generation MODD1 insulin pump to the US Food and Drug Administration (FDA) for 510(k)...
Biocomposites, an international medical devices company that engineers, manufactures and markets world leading products for regenerating bone and managing infection in bone and soft...
Enspectra Health has received FDA 510(k) clearance from the US Food and Drug Administration (FDA) for VIO System, a non-invasive skin imaging technology.
By combining...
US-based medical equipment manufacturer iRhythm Technologies has received the CE mark for its next-generation long-term ambulatory cardiac monitor, Zio monitor ECG system.
The Zio monitor...
US-based medical technology company EndoSound has received the US Food and Drug Administration (FDA) 510(k) approval for its EndoSound Vision System (EVS).
The EVS is...
Israeli medical device company Belkin Vision has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its glaucoma laser, the Eagle...
