Liviwell, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Liviwell, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Livi Device
1
Total
1
Cleared
0
Denied
Liviwell, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mountain Lakes, US.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Liviwell, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory and Technical Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Liviwell, Inc.
1 devices