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Convergent Genomics announced that its non-invasive genomic urine test UroAmp can detect bladder cancer and predict its recurrence before the onset of symptoms, based on data from a
Regenesis Biomedical, Inc., a medical device company focused on safe, non-drug, pain management, announced today commercialization of the new Reprieve by Regenesis™ device (Reprieve). Reprieve is the only
US-based medical device company Exactech has received the US Food and Drug Administration (FDA) 510(k) approval for a new Activit-E polyethylene, used with its Truliant knee replacement system.
Israeli medical device startup Nurami Medical has received the US Food and Drug Administration (FDA) 510(k) approval for its electrospun nanofiber-based product, ArtiFascia Dura Substitute. ArtiFascia is a
Boekel Scientific introduces a new product line that consists of 4 families of centrifuges: economy, general purpose, STAT, and Blood Bank. Boekel Scientific has been manufacturing medical and
Australia-based implantable hearing solutions provider Cochlear has rolled out its next-generation Cochlear Osia System, which enables MRI scanning at 3 Tesla. Initially launched in 2020, the Osia System
Abiomed, a medical device technology company of Johnson & Johnson MedTech, has announced positive results for its Impella heart pump, from a third-party analysis. The data showed that
Perry Health, a prominent healthcare company, is members in Idaho to its diabetes management platform, marking a significant advancement towards ensuring accessible and continuous care for patients throughout the state.
Anika Therapeutics, a US-based provider of tissue protection, healing, and repair products, has received the US Food and Drug Administration 510(k) approval for its Integrity Implant System. The
IMIDEX, a medical device company developing AI-based solutions for lung cancer, has received the US Food and Drug Administration (FDA) 510(k) approval for its VisiRad XR device. VisiRad