The Food and Drug Administration (FDA) has granted 510(k) clearance for Vesalio’s enVast clot retriever, paving the way for ...

US-based Subsense has raised $10m, bringing the brain-computer interface (BCI) developer’s total funding to $27m since it ...

The US Food and Drug Administration (FDA) has cleared Flow Neuroscience’s at-home, non-drug depression treatment, making it ...

Guardant Health and AI technology firm Trial Library have formed a strategic partnership aimed at improving access to cancer ...

Impulse Dynamics has secured over $158m in funding aimed at supporting its commercialisation efforts and progressing its ...

Teleflex is selling its acute care, interventional urology, and original equipment manufacturer (OEM) businesses in two ...

Nitinotes has commenced its US investigational device exemption (IDE) Endoscopic Automated Sleeve Evaluation (EASE) Clinical ...

Medline has filed for an initial public offering (IPO) seeking to raise up to $5.37bn, a figure that would leave the medical ...

Lunit has announced the submission of a 510(k) premarket notification seeking clearance from the US FDA for its breast cancer ...

The US Food and Drug Administration (FDA) has launched Technology-Enabled Meaningful Patient Outcomes (TEMPO), a pilot that ...

Singapore Health Sciences Authority (HSA) has granted approval for Respiree’s 1Bio AI-Acute toolbox, classifying it as a ...

Roche has secured CE Mark approval for its cobas BV/CV assay to support the diagnosis of infectious causes of vaginitis.