Neko Health AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Neko Health AB - FDA 510(k) Cleared Devices
Recent clearances: Spectrum-2, Derma-2
2
Total
2
Cleared
0
Denied
Neko Health AB has 2 FDA 510(k) cleared medical devices. Based in Danderyd, SE.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Neko Health AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Healthcare Innovation Catalysts, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Neko Health AB
2 devices