Medical Device Manufacturer · US , Minneapolis , MN

Novartis Nutrition Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1998

Total

Cleared

Denied

Novartis Nutrition Corp. has 5 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 5 cleared submissions from 1998 to 2008. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Novartis Nutrition Corp. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.

Novartis Nutrition Corp. is one of 16052 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Novartis Nutrition Corp.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 08, 2026