Teleflex Says Arrow EZ-IO Needle Is The First And Only Intraosseous (IO) Needle To Receive 510(k) clearance From FDA For MR Conditional Labeling
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Teleflex's Arrow EZ-IO Needle, a component of the Arrow EZ-IO Intraosseous Vascular Access System, has received 510(k) clearance from the FDA for MR Conditional Labeling. The needle has a patented diamond tip for fast and precise insertion and can be used when intravenous access is difficult or impossible.
June 06, 2023 | 10:35 am
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Teleflex's Arrow EZ-IO Needle has received FDA 510(k) clearance for MR Conditional Labeling, potentially increasing the adoption of the Arrow EZ-IO Intraosseous Vascular Access System.
The FDA 510(k) clearance for Teleflex's Arrow EZ-IO Needle is a significant regulatory milestone for the company. This clearance may lead to increased adoption of the Arrow EZ-IO Intraosseous Vascular Access System, as it demonstrates the safety and effectiveness of the needle. This could potentially lead to increased sales and revenue for Teleflex, positively impacting its stock price in the short term.
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