Medical Device Developments Weekly

Medical Device Developments Weekly

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Welcome to this week's Medical Device Developments newsletter.

See the latest insight and analysis from the global medical device market from the last week below:


OSSIO launches OSSIOfiber compression staples for hand and foot surgeries

?? OSSIO launches OSSIOfiber compression staples for hand and foot surgeries  The American orthopedic fixation company is engaged in developing bio-integrative fixation implants that leave no permanent residue.   The OSSIOfiber small compression staples enhance OSSIO’s portfolio, which includes larger compression staples, suture anchors, trimmable fixation nails, compression screws, and a hammertoe fixation system.  These implants utilise a bio-integrative fiber matrix designed for ease of use and compression strength that matches or exceeds nitinol staples, all without permanent implantation.  Read more online: https://lnkd.in/eTuBgDN8  ?? Follow Medical Device Developments to receive the latest medical device news daily and to subscribe to our weekly newsletter  hashtag#MedicalDeviceDevelopments hashtag#medicaldevices hashtag#medicalmanufacturing

The American orthopedic fixation company is engaged in developing bio-integrative fixation implants that leave no permanent residue.

The OSSIOfiber small compression staples enhance OSSIO’s portfolio, which includes larger compression staples, suture anchors, trimmable fixation nails, compression screws, and a hammertoe fixation system.

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GE HealthCare, MediView XR, Inc. announce first installation and clinical use of OmnifyXR

?? GE HealthCare, MediView XR, Inc. announce first installation and clinical use of OmnifyXR  OmnifyXR is an advanced augmented reality (AR) based interventional radiology suite, developed by MediView XR, Inc. XR, in collaboration with GE HealthCare.  The radiology suite combines a holographic heads-up display streaming live medical imaging, 3D anatomy model visualisation and advanced imaging technologies.  In addition, the solution also enables remote collaboration to help advance the delivery of precision care across a variety of interventional procedures.  Read more online: https://lnkd.in/gF2A3QCr  ?? Follow Medical Device Developments to receive the latest medical device news daily and to subscribe to our weekly newsletter  hashtag#MedicalDeviceDevelopments hashtag#medicaldevices hashtag#medicalmanufacturing

OmnifyXR is an advanced augmented reality (AR) based interventional radiology suite, developed by MediView XR, Inc. XR, in collaboration with GE HealthCare .

The radiology suite combines a holographic heads-up display streaming live medical imaging, 3D anatomy model visualisation and advanced imaging technologies.

Read more


Medtronic, Merit Medical Systems, Inc. expand alliance to offer Kyphon Xpander balloon catheter in US

?? Medtronic, Merit Medical Systems, Inc. expand alliance to offer Kyphon Xpander balloon catheter in US  Currently, Merit Medical Systems, Inc. is supplying Medtronic’s Kyphon Xpander Inflation Syringes used to reduce fractures and create a void in the vertebral body during balloon kyphoplasty procedures.  Under the expanded partnership, Medtronic will carry out the sales, marketing, and distribution of the Kyphon KyphoFlex unipedicular balloon catheter.  Kyphon KyphoFlex is designed to create a controlled, precise, targeted cavity in vertebral augmentation procedures, and complement Medtronic’s current bipedicular solution.  Read more online: https://lnkd.in/gtGb8Kus  ?? Follow Medical Device Developments to receive the latest medical device news daily and to subscribe to our weekly newsletter  hashtag#MedicalDeviceDevelopments hashtag#medicaldevices hashtag#medicalmanufacturing

Currently, Merit Medical Systems, Inc. is supplying Medtronic ’s Kyphon Xpander Inflation Syringes used to reduce fractures and create a void in the vertebral body during balloon kyphoplasty procedures.

Under the expanded partnership, Medtronic will carry out the sales, marketing, and distribution of the Kyphon KyphoFlex unipedicular balloon catheter.

Read more


Why Medical Device Developments is the first choice for medical device manufacturing professionals The authoritative voice of the medical device industry, Medical Device Developments is leading the debate on the evolution of the market through extensive research, data analysis, policy reports and up-to-the-minute reporting from the medical device industry.  Medical Device Developments is the premier information source for the world’s major medical device manufacturers/OEMs to help them make critical business decisions.  Aimed at senior executives, Medical Device Developments provides a clear overview of the latest thinking regarding the role of technology.  Medical Device Developments is supported across a number of platforms online and is positioned as the definitive destination for medical device manufacturing professionals. We are driven by unbiased and authoritative editorial content brought to you by an expert team of journalists with unrivalled industry expertise.

Co-Diagnostics, Inc files FDA 510(k) application for Co-Dx PCR Pro platform

?? Co-Diagnostics, Inc files FDA 510(k) application for Co-Dx PCR Pro platform  The Co-Dx PCR platform aims to address the gap in access to infectious disease diagnostics by enabling widespread decentralisation of polymerase chain reaction testing.  According to Co-Diagnostics, Inc, the platform features a compact, robust real-time PCR instrument designed for use in point-of-care or at-home settings.  It operates through an intuitive smartphone interface and utilises test cups powered by patented Co-Dx Co-Primers technology.  Additionally, Co-Diagnostics, Inc plans to apply soon for the Co-Dx PCR COVID-19 test on this new instrument, intended for point-of-care testing (POCT).  Read more online: https://lnkd.in/eWHH5KHq  ?? Follow Medical Device Developments to receive the latest medical device news daily and to subscribe to our weekly newsletter  hashtag#MedicalDeviceDevelopments hashtag#medicaldevices hashtag#medicalmanufacturing

The Co-Dx PCR platform aims to address the gap in access to infectious disease diagnostics by enabling widespread decentralisation of polymerase chain reaction testing.

According to Co-Diagnostics, Inc , the platform features a compact, robust real-time PCR instrument designed for use in point-of-care or at-home settings.

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CardioFlow Technologies, LLC secures CE mark approval for VitaFlow Liberty system

?? CardioFlow Technologies, LLC secures CE mark approval for VitaFlow Liberty system  VitaFlow Liberty, which prevents open-heart surgery and provides several benefits to patients, is the world’s only electric retrievable transcatheter aortic valve system and is widely used as a preferred choice for aortic heart valve disease.  Before the commercial launch in the EU market, the company conducted pre-market clinical implantations of VitaFlow Liberty in Ireland, Denmark, and the UK.  The clinical implantations were performed at Galway University Hospital in Ireland, Copenhagen University Hospital in Denmark, and St Thomas’ Hospital and NHS Trust in the UK.  Read more online: https://lnkd.in/eEhyyGY5  ?? Follow Medical Device Developments to receive the latest medical device news daily and to subscribe to our weekly newsletter  hashtag#MedicalDeviceDevelopments hashtag#medicaldevices hashtag#medicalmanufacturing

VitaFlow Liberty, which prevents open-heart surgery and provides several benefits to patients, is the world’s only electric retrievable transcatheter aortic valve system and is widely used as a preferred choice for aortic heart valve disease.

Before the commercial launch in the EU market, the company conducted pre-market clinical implantations of VitaFlow Liberty in Ireland, Denmark, and the UK

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Endotronix secures FDA premarket approval for Cordella PA Sensor

?? Endotronix secures FDA premarket approval for Cordella PA Sensor  The Cordella Sensor is an implantable pulmonary artery (PA) pressure sensor that directly measures PA, the indicator of congestion, allowing early, targeted therapy.  It is indicated for patients with New York Heart Failure (NYHA) class 3 heart failure (HF).  The FDA approval was based on the PROACTIVE-HF trial, in which Cordella showed a significantly low rate (0.159) of heart failure hospitalisation and all-cause mortality at 6 months.  Read more online: https://lnkd.in/e6jdh6Zz  ?? Follow Medical Device Developments to receive the latest medical device news daily and to subscribe to our weekly newsletter  hashtag#MedicalDeviceDevelopments hashtag#medicaldevices hashtag#medicalmanufacturing

The Cordella Sensor is an implantable pulmonary artery (PA) pressure sensor that directly measures PA, the indicator of congestion, allowing early, targeted therapy.

It is indicated for patients with New York Heart Failure (NYHA) class 3 heart failure (HF).

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