ABT Berita Forex
Abbott Laboratories Boosts FY24 Earnings Outlook - Update
While reporting financial results for the second quarter on Thursday, Abbott Laboratories (ABT) provided earnings and adjusted earnings guidance for the third quarter and raised its outlook for the full-year 2024.
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103 hari yang lalu
Abbott Says FDA Approves First-of-Its-Kind TriClip Transcatheter Edge-to-edge Repair System
Abbott Laboratories (ABT) announced Tuesday that the U.S. Food and Drug Administration (FDA) has approved the company's first-of-its-kind TriClip transcatheter edge-to-edge repair (TEER) system that's specifically designed for the treatment of tricuspid regurgitation (TR), or a leaky tricuspid valve.
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210 hari yang lalu
Abbott Laboratories Guides FY24 Adj. EPS In Line With Estimates - Update
While reporting financial results for the fourth quarter on Wednesday, Abbott Laboratories (ABT) initiated earnings and adjusted earnings guidance for the full-year 2024.
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279 hari yang lalu
Abbott Inks Deal With MAbxience To Commercialize Biosimilar Molecules In Emerging Markets
Abbott Laboratories (ABT) announced Wednesday an agreement with Spain-based global biotech firm mAbxience Holdings S.L. to commercialize several biosimilars focusing on oncology, women's health and respiratory diseases in emerging markets.
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405 hari yang lalu
Abbott Laboratories Reaffirms FY23 Adj. EPS Outlook - Update
While reporting financial results for the second quarter on Thursday, Abbott Laboratories (ABT) reaffirmed its adjusted earnings guidance for the full-year 2023.
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467 hari yang lalu
Abbott Laboratories Says FDA Approves Assert-IQ Insertable Cardiac Monitor
Abbott Laboratories (ABT) announced Thursday that its Assert-IQ insertable cardiac monitor (ICM) has received U.S. Food and Drug Administration (FDA) clearance, giving physicians a new option for diagnostic evaluation and long-term monitoring of people experiencing irregular heartbeats.
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530 hari yang lalu
Abbott Says FDA Approves Spinal Cord Stimulation Devices To Treat Chronic Back Pain
Abbott Laboratories (ABT) announced Tuesday that the U.S. Food and Drug Administration (FDA) has approved its spinal cord stimulation (SCS) devices for the treatment of chronic back pain in people who have not had or are not eligible to receive back surgery, known as non-surgical back pain.
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532 hari yang lalu
Abbott Announces Two New FDA Clearances For Life Support System
Abbott Laboratories (ABT) announced Tuesday two new clearances from the U.S. Food and Drug Administration (FDA) for the company's industry-leading life support system.
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553 hari yang lalu
Abbott Says FDA Oks Proclaim XR Spinal Cord Stimulation System To Treat DPN
Abbott Laboratories, Inc. (ABT) announced Thursday that the U.S. Food and Drug Administration (FDA) has approved its Proclaim XR spinal cord stimulation (SCS) system to treat painful diabetic peripheral neuropathy (DPN), a debilitating complication of diabetes.
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642 hari yang lalu
Abbott Says FDA Oks Navitor TAVI System To Treat Severe Aortic Stenosis
Abbott Laboratories (ABT) announced Tuesday that the U.S. Food and Drug Administration (FDA) has approved the company's latest-generation transcatheter aortic valve implantation (TAVI) system, Navitor, to treat people with severe aortic stenosis who are at high or extreme risk for open-heart surgery.
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651 hari yang lalu
