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Omeq Medical, a portfolio company of Israel-based Trendlines Group, has received the US Food and Drug Administration (FDA) approval for its EpiFinder smart device. EpiFinder is a sensor-based,
Diagnostic company SphingoTec has been successfully re-certified according to ISO 13485 and received its first IVDR certificate for its IVD product sphingotest® penKid®. The certificates awarded by its
Singlera Genomics, a company focused on non-invasive genetic testing, has received the Food and Drug Administration (FDA) Breakthrough Device Designation for its PDACatch assay. PDACatch is a novel
German medical device company Siemens Healthineers has agreed to distribute Scopio Labs’ full-field digital cell morphology platforms, Scopio X100 and Scopio X100HT. The imaging platforms are intended for
Soterix Medical Inc. (SMI), a global leader in non-invasive stimulation and synergistic brain monitoring technologies, announced today that patient recruitment for its treatment resistant depression trial funded by National Institute of
Danish ophthalmic laser manufacturer Norlase has received both the US Food and Drug Administration (FDA) 510(k) approval and the CE mark for its ECHO Green Pattern Laser photocoagulator.
US-based medical device company Know Labs has announced positive results for its non-invasive glucose monitoring sensor from its recent technical feasibility study. The company conducted a series of
Probo Medical (“Probo”), a leading global provider of medical imaging equipment, parts, repair and service, announced today that it has completed its acquisition of the MRI coil repair
Cognixion has received the US Food and Drug Administration (FDA) Breakthrough Device designation for its brain-computer interface (BCI) technology, Cognixion ONE Axon. Cognixion ONE Axon is an advanced
Cumulus Neuroscience, a digital health company focused on neuroscience, has received the US Food and Drug Administration (FDA) 510(k) approval for its novel dry-sensor EEG headset. The device