Our Center for Devices and Radiological Health qualified a new patient-reported outcome instrument through the Medical Device Development Tools (MDDT) program. The Assessment of IntraOcular Lens Implant Symptoms (AIOLIS) instrument assesses frequency and bother of ocular symptoms in certain patients undergoing intraocular lens implant. Find out more about the new tool. https://lnkd.in/ez73KUmN
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Senior Biomedical Engineer specializing in Medical Device R&D, Regulatory and Quality Management Systems
One of my favorite things to do is share my thoughts on neurovascular devices. It is endlessly fascinating to come across these innovative medical devices. Today, I will share about eCLIPS device - that is used to treat wide-necked bifurcation aneurysms (WNBAs). This device is opens in a leaf shape is useful for treating WNBAs - which are very hard to treat. Why are WNBAs hard to treat? Because WNBAs has a low dome-to-neck ratio, causes any coil/embolic device to slip through and relapse into parent artery!! Traditionally, they have been treating these bifurcation aneurysms with a ‘y-stent technique’ where two intersecting stents are deployed across a bifurcation aneurysm neck. This device can be deployed to prevent this + offer a scaffold for endothelial/neo-intimal growth. Link: https://www.evasc.com/
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📢 ONWARD completes first-in-human implant of ARC-IM Stimulator with BCI The patient received a wireless brain-computer interface (BCI), which enables thought-driven movement when used together with the ARC-IM Stimulator. ONWARD The said that our ARC-IM Stimulator is designed to deliver targeted, programmed ARC-IM Therapy to the spinal cord to restore movement and other functions after spinal cord injury. ARC-IM Therapy has been tested across multiple clinical feasibility studies to restore mobility and stabilise blood pressure after SCI. It is the first application of the ARC-IM Therapy for restoring upper extremity movement and function, The Dutch medical technology company. Read more online: bit.ly/3PQSurn 📰 Follow Medical Device Developments to receive the latest medical device news daily #MedicalDeviceDevelopments #onward #bci #wirelesshealthcare #patientcare #patientmobility #spinalcordinjuries
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BrainScope is the first and only FDA-cleared non-invasive medical device that objectively assesses mild head-injured patients for brain bleeds and concussions. Read more about our technology here: #BrainScope #concussion #BrainHealth #hedainjury https://bit.ly/3P1iVtt
Science & Technology
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Read the latest glaucoma news in the digital edition. In this issue we report news about prior authorizations, Iridex, LumiBird, Nova Eye Medical, and more. https://lnkd.in/gdA2_mAG
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Brief overview of basic wires in the Cath Lab! 0.035 J Wire Wholey Wire by Medtronic Glidewire by Terumo Helpful descriptions you can remember! #cathlab #cathlabequipment #vascular #coronaryarterydisease #heartdisease #medicalequipment
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📢 Boston Scientific gets FDA nod for updated WATCHMAN FLX Pro LAAC device The device is indicated to reduce stroke risk in patients with non-valvular atrial fibrillation (NVAF) who need an alternative to oral anticoagulation therapy. It is an updated version of the previous WATCHMAN FLX LAAC device, which was approved in the US in July 2020, and has been used in nearly 190,000 procedures worldwide. The WATCHMAN FLX Pro is enhanced with a polymer coating designed to reduce device-related thrombus and enable rapid, controlled healing. It comes with additional visualisation markers to enhance the device placement for optimal sealing around the LAA. Also, the US biomedical engineering company offers the WATCHMAN FLX Pro device in a new 40mm size option, enabling physicians to treat a wide range of anatomies. Read more online: bit.ly/3Ev5a0Q 📰 Follow Medical Device Developments to receive the latest medical device news daily #MedicalDeviceDevelopments #bostonscientific #fda #stroke #atrialfibrillation #patientcare #healthcare
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We are volunteers of the Rochester, NY chapter of Mended Hearts. We are heart patients working with heart patients, caregivers and family to help and educate them about heart disease
Interesting article on new medical device to limit esophagus issues with AFIB ablations
President/CEO at RecoverRite and HeartPatientAI | AI-driven Custom CV-Specific Patient Education Solutions | Transplant Patient Education with TransplantPatientAI
New medical device helps cardiologists limit esophageal injuries during RF ablation procedures
New medical device helps cardiologists limit esophageal injuries during RF ablation procedures
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Go beyond triage and notification to provide clinical depth and value for faster, more accurate diagnostic decisions earlier in the #stroke patient journey. Rapid NCCT Stroke is the only, premiere, FDA-approved #AI-based medical device that determines suspicion of ICH and LVO based on non-contrast CT (NCCT) imaging. In tandem with Rapid ICH and Hyperdensity, Rapid ASPECTS and Rapid Hypodensity, #RapidAI is the only complete solution on the market that can help doctors determine which patient should get thrombectomy from NCCT scans.
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There are surgical and percutaneous interventional strategies to treat ASD, each with its own advantages and inevitable drawbacks too. The most common complication is embolization or malposition of device, frequently during the initial hours to the first 24 hours.Important predictors of ASD device embolization are large defects, bigger devices, insufficient rims, undersized device, or insufficient left atrial size to hold a device. #InterestingCase #Transesophageal
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Great news on the improvement!! This advancement indeed highlights the ongoing commitment to enhancing patient outcomes.