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BioWorld - Friday, March 20, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Nov. 5, 2015

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Building Cellular Therapy: Videregen starting first trachea transplant trial with stem cell approach

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New ACDF Product: FDA approves Cerapedics' i-Factor bone graft for cervical fusion

The FDA has approved a biologic bone graft for use in the cervical spine. The i-Factor peptide enhanced bone graft from Cerapedics Inc. (Westminster, Colo.), a private orthobiologics company, was approved as a drug-device combination product for use in anterior cervical disectomy and fusion (ACDF) procedures in patients with degenerative cervical disc disease. The product represents the first FDA-approved bone graft in the cervical spine and the second FDA-approved bone graft in the spine. Read More

Inside the Beltway: Physician groups gang-tackle Congress over meaningful use

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ME panel provides rapid results: FDA nod for new Filmarray panel increases momentum for Biofire Diagnostics

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Third Quarter: BD beats expectations, sees 39.3 percent increase in revenues

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Daily M&A: Intricon Corp. acquires assets of PC Werth Ltd.

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World in Review: Singapore hospital teams with Thermo Fisher in Asian NGS

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Court Report: ICC issues award to Accuray's former Chinese distributor

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Agreements/contracts: Unilife signs injector platform MDSA with Medimmune

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People in places

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Product Briefs

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Briefly noted

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MDD's Orthopedics Extra

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