Solevy Co., LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Solevy Co., LLC - FDA 510(k) Cleared Devices
Recent clearances: Solevy Co. LLC Silicone Based Personal Lubricant, Solevy Co. LLC Water-Based Personal Lubricant
2
Total
2
Cleared
0
Denied
Solevy Co., LLC has 2 FDA 510(k) cleared medical devices. Based in Valencia, US.
Last cleared in 2021. Active since 2021. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Solevy Co., LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Solevy Co., LLC
2 devices