Leana Orders, Inc. is one of 5511 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
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.
510(k) submissions have been managed by Nst Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Leana Orders, Inc.
2 devices