Synthon Hispania S.L. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Synthon Hispania S.L. has 1 FDA 510(k) cleared medical devices. Based in Sant Boi De Llobregat, ES.
Latest FDA clearance: Dec 2024. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Synthon Hispania S.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lachman Consultant Services, Inc. as regulatory consultant.
1 devices