Please provide your email address to receive an email when new articles are posted on . The FDA announced it has authorized marketing of the first laser-based device for the removal of inferior vena ...

The FDA granted breakthrough device designation to Royal Philips NV for its laser-assisted inferior vena cava (IVC) filter removal device. The Amsterdam-based company designed the device to ablate ...

SILVER SPRING, Md., Dec. 21, 2021 /PRNewswire/ -- Today, the U.S. Food and Drug Administration authorized marketing of the first laser-based device for the removal of Inferior Vena Cava (IVC) filters.

The FDA granted breakthrough device designation to Royal Philips NV for its laser-assisted inferior vena cava (IVC) filter removal device. The Amsterdam-based company designed the device to ablate ...

Please provide your email address to receive an email when new articles are posted on . Royal Philips announced the FDA has granted breakthrough device designation for its laser-assisted inferior vena ...

FDA approved the Philips CavaClear Laser Sheath for use with conventional snare devices for the removal of inferior vena cava (IVC) filters, the agency announced on Tuesday. This makes CavaClear the ...

The US Food and Drug Administration (FDA) has cleared for marketing the Philips CavaClear Laser Sheath, the first laser-based device to facilitate removal of inferior vena cava (IVC) filters when ...

FAIRFAX, Va.--The first large-scale, multispecialty prospective clinical research trial to evaluate the use of inferior vena cava (IVC) filters and related follow-up treatment in the United ...