KORU Medical filed a 510(k) to use FreedomEDGE for subcutaneous PHESGO delivery, expanding into oncology and simplifying ...
CV seeks FDA clearance to add AI-based reading to CapsoCam Plus to boost diagnostic accuracy and streamline reviews.
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CapsoVision seeks FDA clearance for AI endoscopy module
CapsoVision, Inc. ( ($CV) ) has shared an announcement. On December 29, 2025, CapsoVision, Inc. announced it had submitted a 510(k) application to ...
Stereotaxis plans to launch the MAGiC cardiac ablation catheter in early 2026, CEO and Chair David Fischel tells MassDevice.
BrainSpace, a medical technology company building automated solutions for neuro injury, illness and degeneration, today announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) ...
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Inspira Technologies moves into liquid biopsy with planned acquisition and $15 million strategic investment
Inspira Technologies Oxy BHN ( ($IINN) ) has issued an announcement. On January 5, 2026, Inspira Technologies Oxy B.H.N. Ltd. signed a non-binding ...
Chicago hospitals and health companies head into 2026 facing reimbursement pressure, rising premiums, uninsured worries and ...
Other World Computing (OWC®), a trusted leader in high-performance storage, memory, connectivity, software, and accessories that empower creative and business professionals to maximize performance, ...
DMedical shares (ASX:4DX) have shown some strong price volatility in recent sessions, with today marking the third session in ...
Ceribell received breakthrough device designation for its LVO stroke detection monitor, and Naox Technologies secured 510(k) clearance for its in-ear EEG device.
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Enhanced wearable builds on Revi’s strong clinical evidence, meaningful symptom relief, and exceptionally high patient satisfaction. SALT LAKE CITY--(BUSINESS WIRE)--BlueWind Medical, Ltd., a leader ...
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