Medical Device Manufacturer · DE , Munich

Livanova Deutschland, GmbH - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2020

Total

Cleared

Denied

Livanova Deutschland, GmbH has 7 FDA 510(k) cleared medical devices. Based in Munich, DE.

Last cleared in 2023. Active since 2020. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Livanova Deutschland, GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by LivaNova USA, Inc. as regulatory consultant.

Livanova Deutschland, GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Livanova Deutschland, GmbH

7 devices

1-7 of 7