Lazarus 3D, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lazarus 3D, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PRE-SURE
1
Total
1
Cleared
0
Denied
Lazarus 3D, Inc. has 1 FDA 510(k) cleared medical devices. Based in Corvallis, US.
Last cleared in 2021. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Lazarus 3D, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Obelix Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Lazarus 3D, Inc.
1 devices