Willow Innovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Willow Innovations, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Willow Generation 3 Breast Pump, Lucy Breast Pump
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Willow Innovations, Inc.
2 devices