Santec Corporation is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Santec Corporation - FDA 510(k) Cleared Devices
Recent clearances: ARGOS
2
Total
2
Cleared
0
Denied
Santec Corporation has 2 FDA 510(k) cleared medical devices. Based in Komaki, JP.
Historical record: 2 cleared submissions from 2015 to 2019. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Santec Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Santec Corporation
2 devices