February 6, 2023

Northeast Scientific Receives FDA Clearance to Reprocess the Eagle Eye Platinum RX Digital IVUS Catheter

February 6, 2023—Northeast Scientific Inc. (NES), a Waterbury, Connecticut–based company that reprocesses single-use peripheral vascular catheters, announced it has received FDA 510(k) clearance for reprocessing the Philips intravascular ultrasound (IVUS) Eagle Eye Platinum RX digital catheter.

The company advised it will soon announce when the NES Reprocessed Eagle Eye Platinum RX digital IVUS catheter device will be available for sale.

In July 2022, NES received clearance of the reprocessed Philips Turbo-Elite laser atherectomy catheter. In 2020, the company announced 510(k) clearance for reprocessing a .014-inch digital IVUS catheter.

NES CEO and Founder, Craig Allmendinger commented in the company’s press release, “The reprocessed Eagle Eye catheter is another high-cost complex interventional device that will bring considerable savings to office-based labs and hospital cath labs nationwide. Having reprocessed multiple sizes of the peripheral IVUS device for the last 3 years to great success, it was an easy choice to pursue the Eagle Eye version.”

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February 6, 2023

Northeast Scientific Receives FDA Clearance to Reprocess the Eagle Eye Platinum RX Digital IVUS Catheter

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