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Home»Posts tagged with»medical devices (Page 4)

Can Chest Wall Innovations turn FDA clearance into adoption in rib fixation?

By Pallavi Madhiraju on April 30, 2026   Medical Devices & Diagnostics  

Can Chest Wall Innovations turn FDA clearance into adoption in rib fixation?

Rib fixation is gaining clinical ground. Chest Wall Innovations now faces the harder test: converting FDA clearance into surgeon adoption.

Why Abbott’s Ultreon 3.0 could reshape stent planning in complex coronary disease

By Pallavi Madhiraju on April 29, 2026   Medical Devices & Diagnostics  

Why Abbott’s Ultreon 3.0 could reshape stent planning in complex coronary disease

AI can now guide coronary imaging in real time. Abbott’s Ultreon 3.0 puts precision PCI closer to routine clinical workflow.

Why Pulse Biosciences’ 12-month nsPFA data matters in a PFA market dominated by Farapulse and Affera

By Pallavi Madhiraju on April 26, 2026   Medical Devices & Diagnostics  

Why Pulse Biosciences’ 12-month nsPFA data matters in a PFA market dominated by Farapulse and Affera

Boston Scientific owns the PFA market. Pulse Biosciences just posted 90% one-year AF freedom. Is nanosecond PFA a real disruption or an acquisition target?

Can Utepreva’s new device solve the biggest problem in endometrial cancer diagnosis?

By Pallavi Madhiraju on April 24, 2026   Medical Devices & Diagnostics  

Can Utepreva’s new device solve the biggest problem in endometrial cancer diagnosis?

Utepreva’s FDA-cleared endometrial sampler promises earlier cancer detection. Find out how this device could reshape diagnostics today.

Medtronic backs Pulnovo Medical in $100m round to expand PADN in pulmonary hypertension

By Pallavi Madhiraju on April 20, 2026   Medical Devices & Diagnostics  

Medtronic backs Pulnovo Medical in $100m round to expand PADN in pulmonary hypertension

Pulnovo Medical raised $100 million with Medtronic backing. Read what it means for PADN, pulmonary hypertension, heart failure, and device markets.

Why Miracell’s SMART M-CELL FDA clearance could reshape the PRP and BMAC device market

By Pallavi Madhiraju on April 11, 2026   Medical Devices & Diagnostics  

Why Miracell’s SMART M-CELL FDA clearance could reshape the PRP and BMAC device market

Miracell has won FDA 510(k) clearance for SMART M-CELL. Read what it changes for PRP, BMAC, adoption, and regenerative medicine competition.

Why InterVene’s first 30 Recana cases could reshape treatment for venous in-stent restenosis

By Pallavi Madhiraju on April 8, 2026   Medical Devices & Diagnostics  

Why InterVene’s first 30 Recana cases could reshape treatment for venous in-stent restenosis

InterVene has completed 30 Recana cases, raising new questions about venous ISR treatment, adoption, and launch strategy. Read the full analysis.

Can VR LIFE and H2 Global Group turn European MedTech validation into real global scale?

By Pallavi Madhiraju on April 4, 2026   Medical Devices & Diagnostics  

Can VR LIFE and H2 Global Group turn European MedTech validation into real global scale?

Can VR LIFE and H2 Global Group scale from European validation to global MedTech relevance? Read the deeper analysis now.

Can Allevion Medical’s Vantage change spinal stenosis workflows by combining disposable access, illumination, and bone resection tools?

By Pallavi Madhiraju on April 4, 2026   Medical Devices & Diagnostics  

Can Allevion Medical’s Vantage change spinal stenosis workflows by combining disposable access, illumination, and bone resection tools?

Allevion Medical’s Vantage won FDA 510(k) clearance for lumbar decompression. Read what this may change for spinal stenosis workflow, adoption, and risk.

How ATL Medical’s PREVOYANCE imaging system could speed arthroscopy device development with OMNIVISION’s OH0131 processor

By Pallavi Madhiraju on April 4, 2026   Medical Devices & Diagnostics  

How ATL Medical’s PREVOYANCE imaging system could speed arthroscopy device development with OMNIVISION’s OH0131 processor

ATL Medical and OMNIVISION have expanded arthroscopy imaging integration. Read what this means for OEM speed, quality, and device development.

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