iMediSync, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
iMediSync, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iSyncBrain©-C, iSyncWave
2
Total
2
Cleared
0
Denied
iMediSync, Inc. has 2 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Last cleared in 2023. Active since 2022. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by iMediSync, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - iMediSync, Inc.
2 devices