Teleflex Receives FDA 510 (k) Clearance of the AC3 Range™ Intra-Aortic Balloon Pump (IABP) Teleflex Incorporated - GlobeNewswire - Tue Apr 1, 5:30AM CDT ...

Dive Insight: The recall affects nearly 17,000 intra-aortic balloon catheter kits that Teleflex and its subsidiary Arrow International distributed in the U.S. between May 2022 and April 2024.

WAYNE, Pa., April 01, 2025 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced FDA 510 (k) clearance of the AC3 Range Intra-Aortic ...

Limerick, Pa.-based Teleflex announced it was awarded a new agreement from Novation for its complete line of Arrow Intra-Aortic Balloon Catheters and Pumps. The agreement, effective Jan. 1, 2014, will ...

WAYNE, Pa., April 01, 2025 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced FDA 510(k) clearance of the AC3 Range™ Intra ...

The addition to the IABP family supports uncompromised cardiac support for patients during transport WAYNE, Pa., April 01, 2025 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE: TFX), a leading global ...

--Teleflex Incorporated, a leading global provider of medical technologies, today announced FDA 510 clearance of the AC3 Range™ Intra-Aortic Balloon Pump. Christopher Buller, MD, Medical ...

"For nearly 40 years, Teleflex has been committed to advancing intra-aortic balloon pumping, delivering cardiac support for critically ill patients,” said Roger Graham, President and General ...