AngioDynamics, Inc. - FDA 510(k) Cleared Devices

AngioDynamics, Inc. is a global leader in vascular and oncology medical technologies, with a manufacturing facility in Glens Falls, US. The company develops advanced devices addressing blood flow restoration, cancer therapies, vascular access, and varicose vein treatment.

AngioDynamics has received 82 FDA 510(k) clearances from 87 total submissions since its first clearance in 1995. The company specializes in cardiovascular devices, with recent cleared products including mechanical aspiration systems, infusion systems, and angiographic catheters. The latest FDA 510(k) clearance was granted in 2025, demonstrating continued regulatory activity and product innovation.

The company's device portfolio spans multiple therapeutic areas including vascular intervention, oncology support, and minimally invasive procedures. AngioDynamics maintains an active presence in the medical device market with ongoing FDA submissions and clearances.

Explore the complete list of device names, product codes, and clearance dates in the 510(k) database to review AngioDynamics' full regulatory history and cleared products.

1 device has linked clinical trial registered on ClinicalTrials.gov.