Hidroxa Medical AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Hidroxa Medical AB - FDA 510(k) Cleared Devices
Recent clearances: Hidroxa SE30
1
Total
1
Cleared
0
Denied
Hidroxa Medical AB has 1 FDA 510(k) cleared medical devices. Based in Partille, SE.
Latest FDA clearance: Oct 2024. Active since 2024. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Hidroxa Medical AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hidroxa Medical AB
1 devices