
Nordic Kinetics Receives FDA 510(k) Clearance for Parkinson's Disease Monitoring18.6.2026 14:02:57 CEST | Nordic Kinetics AB | Pressmeddelande
Nordic Kinetics AB has received 510(k) clearance from the U.S. Food and Drug Administration for its Sine Monitoring application, a software as a medical device (SaMD) running on Apple Watch that quantifies tremor and dyskinesia in adults with Parkinson's disease. It is the company's first FDA 510(k) cleared product on its Sine Monitoring platform for movement disorders.


















