Implicity, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Implicity, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SignalHF (IM008), IM007
3
Total
3
Cleared
0
Denied
Implicity, Inc. has 3 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Latest FDA clearance: Jul 2026. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Implicity, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mj Medtech Consulting Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Implicity, Inc.
3 devices