Who doesn't love getting the latest tech for the holidays? It's the perfect time to unwind with some of your favorite games, after all. Whether you want to treat yourself or make that special gamer in ...
Denali Therapeutics Inc. announced that The FDA granted the BLA Priority Review with a Prescription Drug User Fee Act (PDUFA) target action date of January 5, 2026. Coya Therapeutics Enters 2026 With ...
This year’s flu season is shaping up to be a nasty one—driven by a new variant of the influenza virus that may be able to slip past our vaccine defenses. A mutated form of the influenza A strain H3N2 ...
Welldoc Builds on its Foundation of 11 Prior FDA 510(k) Clearances with a Generative AI Model Submission Welldoc®, a leader in AI-powered cardiometabolic health solutions, today announced the ...
Here are 40 spine devices and technologies earning FDA clearances in 2025. Note: This is not an exhaustive list. 1. SurGenTec earned FDA 510(k) clearance for its OsteoFlo HydroFiber to be used as a ...
MAHWAH, N.J.--(BUSINESS WIRE)--KORU Medical Systems, Inc. (NASDAQ: KRMD) (“KORU Medical” or the “Company”), a leading medical technology company focused on the development, manufacturing, and ...
KORU Medical Systems, Inc. (NASDAQ: KRMD) (“KORU Medical” or the “Company”), a leading medical technology company focused on the development, manufacturing, and commercialization of innovative and ...
NEW YORK – Italian in vitro diagnostics firm Diasorin said on Sunday that the US Food and Drug Administration has issued 510(k) clearance and CLIA-waived the firm's first assay for use on the Liaison ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results