Abionic SA is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Abionic SA - FDA 510(k) Cleared Devices
Recent clearances: IVD CAPSULE PSP
1
Total
1
Cleared
0
Denied
Abionic SA has 1 FDA 510(k) cleared medical devices. Based in Epalinges, CH.
Latest FDA clearance: Sep 2024. Active since 2024. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Abionic 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 - Abionic SA
1 devices