Wsaud A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Wsaud A/S - FDA 510(k) Cleared Devices
Recent clearances: WSA Self-Fitting Hearing Aid Gen 2, Vibe SF Self-Fitting Hearing Aid
2
Total
2
Cleared
0
Denied
Wsaud A/S has 2 FDA 510(k) cleared medical devices. Based in Lynge, DK.
Latest FDA clearance: Feb 2024. Active since 2022. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Wsaud A/S Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Wsaud A/S
2 devices