Eden Spine, LLC is one of 18445 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eden Spine, LLC - FDA 510(k) Cleared Devices
Recent clearances: Sphynx™, GIZA(R) VERTEBRAL BODY REPLACEMENT
2
Total
2
Cleared
0
Denied
Eden Spine, LLC has 2 FDA 510(k) cleared medical devices. Based in Apple Valley, US.
Historical record: 2 cleared submissions from 2012 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Eden Spine, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Novus Management Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Eden Spine, LLC
2 devices