NEW YORK – BioMérieux announced on Tuesday that it has submitted two gastrointestinal panels to the US Food and Drug Administration for 510(k) review. The BioFire FilmArray Gastrointestinal 1.1 Panel ...

Anchor Point Tracking, designed for use with the new RefleXion X2 platform, underpins SCINTIX therapy with higher fidelity biologic data. "Anchor Point Tracking represents the next major advancement ...

WARRENDALE, Pa., June 23, 2026 (GLOBE NEWSWIRE) -- ECM Therapeutics announced today that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance (K253521) for ECMT-100 WMD, a flowable ...

NEW YORK--(BUSINESS WIRE)--Pathway Labs today announced its public launch of EchoNext, the world’s first FDA-approved AI detection tool that reads standard 12-lead electrocardiograms (ECGs) to flag ...

This clearance represents the first implementation of Masimo’s OIRD detection capability in a hospital monitoring solution. By combining the trusted signal quality of best-in-class Masimo SET® with AI ...

Dimensions (mm) 265.43 x 356.98 x 18.60 300.00 x 203.00 x 38.10 Weight (kg) 2.49 1.2 ...

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ISSOIRE, France--(BUSINESS WIRE)--Regulatory News: BIOCORP (FR0012788065 – ALCOR / Eligible PEA‐PME), a French company specialized in the design, development, and manufacturing of innovative medical ...