Clarimedex, Inc. is one of 26072 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Clarimedex, Inc. has 1 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Clarimedex, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Clarimedex, Inc.
1 devices