Compex Technologies, Inc. is one of 24154 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Compex Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: STAODYN MAX PRESET, MODEL 4470, REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S
2
Total
2
Cleared
0
Denied
Compex Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in New Brighton, US.
Historical record: 2 cleared submissions from 2005 to 2007. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Compex Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Compex Technologies, Inc.
2 devices