AngioDynamics, Inc.

AngioDynamics, Inc. holds 87 FDA 510(k) medical device clearances, first cleared 1995, most recent 2025, with 99 FDA device recalls on record.

Top product codes for AngioDynamics, Inc.

FDA recalls by AngioDynamics, Inc.

10 most recent of 99

Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.

Recent clearances by AngioDynamics, Inc.

Data sourced from openFDA. This site is unofficial and independent of the FDA.