Medical Device Manufacturer · DE , Wurmlingen

Eit Emerging Implant Technologies GmbH - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2017

Total

Cleared

Denied

Eit Emerging Implant Technologies GmbH has 5 FDA 510(k) cleared medical devices. Based in Wurmlingen, DE.

Historical record: 5 cleared submissions from 2017 to 2020. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Eit Emerging Implant Technologies GmbH Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Depuy Synthes Spine and Musculoskeletal Clinical Regulatory Advisers, LLC.

Eit Emerging Implant Technologies 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 - Eit Emerging Implant Technologies GmbH

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: May 28, 2026