Mar 28, 2024
TELA Bio Launched FDA-approved Hernia Mesh Fixation Devices On March 21, 2024, TELA Bio, Inc., a medical technology firm, launched its FDA-approved LIQUIFIX devices for hernia repairs in the United States. The LIQUIFIX FIX8™ and LIQUIFIX Precision™ are specifically engineered for laparoscopic and open femo...
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The Next Wave of Radioligand Therapies: 5 Candidates to Watch
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Emerging TIL Therapies Poised to Broaden the Landscape Beyond AMTAGVI
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BYSANTI Approval Positions Vanda to Compete in the Antipsychotic Market
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