FDA clears CMR Surgical’s Versius Plus robot
CMR Surgical has secured US Food and Drug Administration (FDA) clearance for its Versius Plus minimally invasive robotic surgical system, …
CMR Surgical has secured US Food and Drug Administration (FDA) clearance for its Versius Plus minimally invasive robotic surgical system, …
The UK’s Royal Hospital for Neuro-disability and the East Kent Hospitals University NHS Foundation Trust have tapped Sanome’s MEMORI platform …
Zimmer Biomet has entered an exclusive partnership with OneStep, a digital fall prevention and mobility intelligence platform, to deliver a …
Philips has agreed to acquire SpectraWAVE, a Massachusetts-based medical device company focused on technologies to help diagnose and guide treatment …
Thermedical has treated the first patient in a pivotal clinical trial of its saline-enhanced radiofrequency (SERF) ablation system, used in …
France-headquartered May Health has secured a European CE mark for its Anavi system to address infertility in women with polycystic …
The US Food and Drug Administration (FDA) is removing a limitation on the use of real-world evidence (RWE), clearing the …
The US Food and Drug Administration (FDA) has granted approval for Dilon Technologies’ MarginProbe 2, a next-generation intraoperative margin assessment …
Helio Genomics and LiverRight have entered a partnership to improve access to early liver cancer detection in the US. The collaboration …
Advita Ortho, a global medical technology company, has won the Innovation award in the 2025 Medical Device Network Excellence Awards …
Olympus Corporation has committed $150m to a new venture capital (VC) fund, aiming to deploy the capital to promising medtech …
Philips has signed a deal to acquire enhanced vascular imaging (EVI) product developer SpectraWAVE, expanding the Dutch medtech giant’s minimally …
Vaxxas has received a manufacturing licence from Australia’s Therapeutic Goods Administration (TGA) for its high-density microarray patch (HD-MAP) for clinical …
The US Food and Drug Administration (FDA) has granted approval to P&F USA to begin the randomised, controlled TRICAV II …
Israel-based Bendit Technologies’ steerable microcatheter has gained clearance from the US Food and Drug Administration (FDA), providing US clinicians with …