Novo Nordisk A/S is one of 25927 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novo Nordisk A/S - FDA 510(k) Cleared Devices
Recent clearances: INNOVO
1
Total
1
Cleared
0
Denied
Novo Nordisk A/S, is a global pharmaceutical and healthcare company with a manufacturing facility in Princeton, US. The company develops and manufactures medicines and medical devices across multiple therapeutic areas.
Novo Nordisk received 1 FDA 510(k) clearance from 1 total submission in the General Hospital device category. The company's cleared device, INNOVO, was approved in 2001. This represents a historical regulatory record; the company has not received FDA 510(k) clearances in more than two decades and should be treated as an inactive filer in the medical device space.
Explore the company's device names, product codes, and clearance dates in the full 510(k) database record.
FDA 510(k) Regulatory Record - Novo Nordisk A/S
1 devices