Angiodynamics - FDA 510(k) Cleared Devices

Angiodynamics, is a global leader in vascular and oncology medical technologies, with a manufacturing facility in Marlborough, US. The company develops advanced devices addressing blood flow restoration, cancer treatment, and vascular interventions.

AngioDynamics has received 3 FDA 510(k) clearances from 3 total submissions since its first clearance in 2014. The company's cleared devices span Gastroenterology & Urology, Cardiovascular, and General & Plastic Surgery categories. The latest clearance in 2026 confirms continued regulatory activity and product innovation.

The company's portfolio includes technologies for minimally invasive vascular access, oncology interventions, and blood flow management. These devices support clinical applications ranging from cancer therapy to vascular restoration and port placement procedures.

Explore the complete regulatory record, including device names, product codes, and clearance dates in the 510(k) database.