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Author Archives: Natalie Themm

Xenter, the World’s First “TechMed” Company, Unveils the XenFI Wireless Network

Xenter unveiled XenFI™, the first product in its wireless “Technology in Medicine” ecosystem.

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Multi-Center Liquid Embolic Study Concludes

Completion of Trial is a Sign of Things to Come for Novel Embolic Agent

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Excess Equipment Sale for BioUtah Members

Excess Equipment Sale for BioUtah Members

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FDA Clears Xenocor’s Saberscope, the World’s First Single-use 5mm Laparoscope with Auto-Focus

FDA Clears World’s First Single-use 5mm Laparoscope with Auto-Focus

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Merit Medical Launches the TEMNO Elite™ Soft Tissue Biopsy System

Advanced device offers 72% larger samples, simplifies tissue retrieval, and enhances patient safety

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AAV5 DetectCDx™ Kit Is First ARUP Test Developed to Support a New Therapy

The European Commission’s approval of a novel gene therapy for severe hemophilia A has paved the way for use of a companion diagnostic in the European Union (EU).

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Dynatronics Corporation Reports Fourth Quarter and Fiscal Year 2022 Financial Results and Business Highlights

Dynatronics reported financial results for its fourth quarter and fiscal year ended June 30, 2022, and provided an update on recent business highlights.

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nView s1 reaches its 100th surgery

The nView s1 has just surpassed its landmark 100th clinical case with the help of 22 surgeons at six leading pediatric facilities, including three of the top 10 facilities in the nation.

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EDWARDS LAUNCHES SAPIEN 3 ULTRA RESILIA VALVE FOLLOWING FDA APPROVAL

Edwards Lifesciences announced the launch of the SAPIEN 3 Ultra RESILIA valve, which incorporates Edwards’ breakthrough RESILIA tissue technology with the industry-leading SAPIEN 3 Ultra transcatheter aortic heart valve.

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PolarityTE Reports Second Quarter 2022 Financial Results and Provides Business Update

PolarityTE provided a business update and reported financial results for the quarterly period ended June 30, 2022.

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Co-Diagnostics, Inc. Reports Second Quarter 2022 Financial Results

Second quarter results impacted by volume declines; Further progress on the development of the Co-Dx PCR Home platform

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Sumitomo Pharma Oncology Receives Orphan Drug Designation for DSP-5336, an Investigational Menin and Mixed-Lineage Leukemia Binding Protein for Treatment of Acute Myeloid Leukemia

The U.S. Food and Drug Administration (FDA) granted Orphan Drug Designation for DSP-5336.

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