Neko Health AB is one of 57 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Neko Health AB - FDA 510(k) Cleared Devices
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: Radiology.
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.
Neko Health AB — FDA 510(k) Products and Clearance History
2 devices
Cleared
May 22, 2026
Spectrum-2
General & Plastic Surgery
151d
Cleared
May 20, 2026
Derma-2
Radiology
163d