Medical Device Manufacturer · US , Alexandria , VA

Lansinoh Laboratories - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022

Total

Cleared

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) cleared devices by Lansinoh Laboratories

2 devices

1-2 of 2