Orthodynamix, LLC is one of 20571 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthodynamix, LLC - FDA 510(k) Cleared Devices
Recent clearances: ARTHROSTEER ABLATOR & COAGULATOR, MODELS: REF 1070 & 1080
1
Total
1
Cleared
0
Denied
Orthodynamix, LLC has 1 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Orthodynamix, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Orthodynamix, LLC
1 devices