Imediplus, Inc. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Imediplus, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cardiart Electronic Stethoscope Model DS101 Omni-Steth Electronic Stethoscope Model Omni-Steth, Electronic Stethoscope DS3011A
3
Total
3
Cleared
0
Denied
Imediplus, Inc. has 3 FDA 510(k) cleared medical devices. Based in Chubei City, TW.
Historical record: 3 cleared submissions from 2016 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Imediplus, Inc. 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 - Imediplus, Inc.
3 devices