FDA Clearance for AC3 Intra-Aortic Balloon Pump
The AC3 range Intra-Aortic Balloon Pump received 510(k) clearance from the FDA, allowing for full market release in the U.S. and shipping to customers in Q2 2025.
Strong Performance in Vascular Access
Vascular Access revenue increased by 1.9% year-over-year to $182.4 million, led by strong growth in PICCs and solid performance in EZ-IO.
Ringer Perfusion Balloon Catheter IDE Study Results
Preliminary results for the Ringer PBC Catheter IDE Study were favorable, with a 73% primary efficacy endpoint success rate, supporting a premarket application submitted to the FDA.
Strategic Separation and Acquisition
Intention to separate Teleflex into two companies to enhance shareholder value, and acquisition of BIOTRONIK Vascular Intervention business to close by Q3 2025.
Accelerated Share Repurchase Program
Completed a $300 million accelerated share repurchase program, acquiring over 2.2 million shares at an average price of $135.23.