Medical Device Manufacturer · US , West Columbia , SC

Nephron Nitrile, LLC - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2023

Total

Cleared

Denied

Nephron Nitrile, LLC has 3 FDA 510(k) cleared medical devices. Based in West Columbia, US.

Latest FDA clearance: Mar 2024. Active since 2023. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Nephron Nitrile, LLC Filter by specialty or product code using the sidebar.

Nephron Nitrile, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Nephron Nitrile, LLC

3 devices

1-3 of 3