Leana Orders, Inc. is one of 16306 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Leana Orders, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Grivamax Family of Lasers, Models 272 and 148, Grivamax Hair Growth System
2
Total
2
Cleared
0
Denied
Leana Orders, Inc. has 2 FDA 510(k) cleared medical devices. Based in Staten Island, US.
Last cleared in 2021. Active since 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Leana Orders, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Nst Consulting, LLC and Nst Consultants, Inc..
FDA 510(k) Regulatory Record - Leana Orders, Inc.
2 devices