Newsroom

Fresenius Kabi, an operating company of Fresenius, announced today that it has submitted a 510(k) notification to the U.S. Food and Drug Administration seeking clearance of the Aurora Xi Plasmapheresis System software version 2.0.

Fresenius Kabi, an operating company of Fresenius, received a Novaplus Program Excellence Award from Vizient, Inc., the nation’s largest provider-driven healthcare performance improvement company. The recognition was announced at the Vizient Connections Summit in Las Vegas.

Fresenius Kabi, an operating company of Fresenius, announced today that the Centers for Medicare and Medicaid Services (CMS) issued a permanent, product-specific billing code and granted pass-through payment status for Tyenne® (tocilizumab-aazg).

Fresenius Kabi, an operating company of Fresenius, today named 12 new inductees into the National Blood Donation Hall of Fame. Nominated by blood centers across the U.S., the honorees were chosen for their extraordinary commitment to donating blood or for encouraging blood donation.

Cellular Origins and Fresenius Kabi, an operating company of Fresenius, announces today they have signed a development agreement that leverages each company’s expertise in cell and gene therapies (CGTs).

Fresenius Kabi, an operating company of Fresenius, specializing in biopharmaceuticals, clinical nutrition, medical technologies, and I.V. generic drugs for critical and chronic conditions, and Formycon AG, a leading, independent developer of high-quality biosimilars, announced today that the United States (U.S.) Food and Drug Administration (FDA) has approved OtulfiTM (ustekinumab-aauz), its ustekinumab biosimilar referencing Stelara® ** (ustekinumab). OtulfiTM is approved for the treatment of Crohn’s disease, ulcerative colitis, moderate to severe plaque psoriasis and active psoriatic arthritis. Fresenius Kabi is further continuing its momentum, striving at expanding its strong Biopharma platform, which is a substantial cornerstone of #FutureFresenius.