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

Artivion, Inc. is a biomedical company advancing aortic and cardiovascular technologies. The company operates with a manufacturing facility in Kennesaw, Georgia.

Artivion has received 1 FDA 510(k) clearance from 1 total submission. The company specializes in cardiovascular devices, with its regulatory activity spanning 2025. The latest clearance in 2025 demonstrates continued innovation in this critical medical device category.

Recent cleared devices include pulmonary valve and conduit systems designed for surgical cardiovascular applications. These products reflect the company's focus on advanced tissue-based solutions for cardiac repair and reconstruction.

Explore the company's cleared device names, product codes, and clearance dates in the database above.