Resnent, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Resnent, LLC - FDA 510(k) Cleared Devices
Recent clearances: Outlook Surgical Versa One System (8900139)
1
Total
1
Cleared
0
Denied
Resnent, LLC has 1 FDA 510(k) cleared medical devices. Based in Bloomington, US.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Resnent, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mededge Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Resnent, LLC
1 devices