Neodynamics AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Neodynamics AB - FDA 510(k) Cleared Devices
Recent clearances: NeoNavia Biopsy System
1
Total
1
Cleared
0
Denied
Neodynamics AB has 1 FDA 510(k) cleared medical devices. Based in Lidingo, SE.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Neodynamics AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Neodynamics AB
1 devices