Nipro Technical Solutions, Incoporated is one of 13015 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nipro Technical Solutions, Incoporated - FDA 510(k) Cleared Devices
Recent clearances: Nipro Dry Acid Concentrate Mixer
1
Total
1
Cleared
0
Denied
Nipro Technical Solutions, Incoporated has 1 FDA 510(k) cleared medical devices. Based in Mesa, US.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Nipro Technical Solutions, Incoporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nipro Technical Solutions, Incoporated
1 devices