Lansinoh Laboratories is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lansinoh Laboratories - FDA 510(k) Cleared Devices
Recent clearances: Compact Wearable Pump, Smartpump 3.0 Double Electric Breast Pump
2
Total
2
Cleared
0
Denied
Lansinoh Laboratories has 2 FDA 510(k) cleared medical devices. Based in Alexandria, US.
Last cleared in 2023. Active since 2022. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Lansinoh Laboratories Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lansinoh Laboratories
2 devices