Inmedix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inmedix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CloudHRV™ System (100-01-001)
1
Total
1
Cleared
0
Denied
Inmedix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Normandy Park, US.
Latest FDA clearance: Jan 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Inmedix, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Daniel & Daniel Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Inmedix, Inc.
1 devices