WAYNE, Pa., Aug. 21, 2023 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced the release of the Arrow™ ErgoPack™ Complete Kits ...

Teleflex Corporation TFX recently announced that the FDA has granted 510(k) clearance to e Arrow EZ-IO Needle — the first and only intraosseous (IO) needle — for MR Conditional labeling. The ...

Teleflex and its subsidiary Arrow International recently announced the Class I recall of its Arrow QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits after potential ...

LIMERICK, Pa.--(BUSINESS WIRE)--Teleflex Incorporated (NYSE:TFX), a leading global provider of medical devices for critical care and surgery, has announced it has received FDA 510(k) clearance to ...

WAYNE, Pa.--(BUSINESS WIRE)--Teleflex Incorporated (NYSE:TFX), a global provider of medical devices for critical care and surgery, announced today that its ARROW Endurance™ Extended Dwell Peripheral ...

Arrow FlexBlock will help clinicians to better manage the spread of anesthetic due to its tip design. The product is expected to be preferred by clinicians who turn to ultrasound-guidance to ratify ...

The FDA posted a recall announcement for two catheter kits made by Arrow International LLC, a subsidiary of Wayne, Pa.-based Teleflex Inc., due to problems with the connectors used in the kits. While ...

The ARROW FlexBlock catheter from Teleflex received 501(k) clearance from the FDA, according to News Medical. The Arrow FlexBlock is a continuous peripheral nerve block catheter that is intended for ...