Best of the Best Skin Condition Diagnostic Tools 2026
Spread the loveIntroduction: The Evolution of Skin Diagnostics As we advance into 2026, the landscape of dermatological diagnostics has undergone a remarkable transformation. Driven by technological innovations and a deeper understanding of skin health, professionals now have access to a plethora…
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Terumo announces US FDA clearance for OpusWave imaging system
Terumo Interventional Systems has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its OpusWave dual-sensor imaging system.
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Investor pressure may be driving risky AI medical device launches | Hub
Study finds an association between publicly traded companies and recalls of AI-based medical tools…
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One-of-a-kind: Industrial design and engineering collaboration at Auburn University leads to groundbreaking medical device
/PRNewswire/ — Students from Auburn University’s Mechanical Engineering and Industrial Design programs recently witnessed something pretty special: the public…
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Dental measuring technology earns FDA clearance
Dental technology company Perimetrics has received FDA clearance for its InnerView System. The system is the first FDA-cleared technology that is designed to measure both internal and external mobility in teeth and implants, according to an Oct.
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FDA Grants De Novo Approval for Home Use of Prenatal Ultrasound Platform | Diagnostic Imaging
Already in use in multiple countries, the Pulsenmore ES ultrasound platform reportedly enables expectant mothers to transmit ultrasound video clips through a smartphone app for remote interpretation.
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FDA Clears Plaque Assessment Software for Coronary CT Angiography | Diagnostic Imaging
The AI-powered cvi42 | Plaque software enables adjunctive on-site interpretation of coronary CT angiography (CCTA) scans for plaque quantification.
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Sirona Medical Gets FDA Nod for Advanced Imaging Suite | Diagnostic Imaging
Expanded capabilities for the Sirona Advanced Imaging Suite reportedly include quantitative SUV analysis and multiplanar reconstruction for PET/CT imaging.
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Mode Sensors Receives FDA 510(k) for Fluid Monitoring System
OSLO, Norway–(BUSINESS WIRE)–Mode Sensors (www.modesensors.com) announced today that its Re:Balans hydration monitoring system has received 510(k) clearance from the U.S. Food and Drug Administration, positioning the company to enter the American market with its wearable sensor technology. The clearance allows Re:Balans to be marketed in the United States for non-invasive monitoring of adult patients with fluid management-related health conditions, including those with fluid overload such as
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FDA Grants HemoSonics 510(k) Clearance to Expand Use of Its Quantra Hemostasis System to Obstetric Procedures
DURHAM, N.C.–(BUSINESS WIRE)– #Childbirth–FDA Grants HemoSonics 510(k) Clearance to Expand Use of Its Quantra Hemostasis System to Obstetric Procedures
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