Medical Device Manufacturer · US , Mountain View , CA

Willow Innovations, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022

Total

Cleared

Denied

Willow Innovations, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mountain View, US.

Last cleared in 2023. Active since 2022. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Willow Innovations, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Willow Innovations, Inc.

2 devices

1-2 of 2