Novus Scientific AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Novus Scientific AB - FDA 510(k) Cleared Devices
Recent clearances: TIGR Matrix Surgical Mesh, TIGR Surgical Mesh
2
Total
2
Cleared
0
Denied
Novus Scientific AB has 2 FDA 510(k) cleared medical devices. Based in Uppsala, SE.
Historical record: 2 cleared submissions from 2017 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Novus Scientific AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Cygnus Regulatory, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Novus Scientific AB
2 devices