Medical Device Manufacturer · DE , Wurmlingen

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

5 submissions · 5 cleared · Since 2017

Recent clearances: EIT Cellular Titanium Cervical Cage, EIT Cellular Titanium ALIF Cage, EIT Cellular Titanium TLIF Cage, EIT Cellular Titanium LLIF Cage, EIT Cellular Titanium T/PLIF Cage, EIT Cellular Titanium Lumbar Cage - T/PLIF, EIT Cellular Titanium® Lumbar Cage LLIF

View 5 510(k) Devices ↓

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 Musculoskeletal Clinical Regulatory Advisers, LLC, Musculosketal Clinical Regulatory Advisors, LLC and Depuy Synthes Spine.

Eit Emerging Implant Technologies GmbH is one of 516 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.