Natureplex, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Natureplex, LLC - FDA 510(k) Cleared Devices
Recent clearances: Natureplex Warm Touch Warming Jelly
2
Total
2
Cleared
0
Denied
Natureplex, LLC has 2 FDA 510(k) cleared medical devices. Based in Memphis, US.
Historical record: 2 cleared submissions from 2005 to 2018. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Natureplex, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Natureplex, LLC
2 devices