Dt Medtech, LLC is one of 20080 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dt Medtech, LLC - FDA 510(k) Cleared Devices
Recent clearances: Hintermann Series H2 Total Ankle System
1
Total
1
Cleared
0
Denied
Dt Medtech, LLC has 1 FDA 510(k) cleared medical devices. Based in Towson, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Dt Medtech, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dt Medtech, LLC
1 devices