Medical Device Manufacturer · US , Bloomington , IL

Resnent, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
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
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