Withings SA is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Withings SA - FDA 510(k) Cleared Devices
Recent clearances: Scan Monitor
1
Total
1
Cleared
0
Denied
Withings SA has 1 FDA 510(k) cleared medical devices. Based in Issy-Les Moulineaux, FR.
Last cleared in 2021. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Withings SA Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Withings SA
1 devices