Dne, LLC is one of 20174 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dne, LLC - FDA 510(k) Cleared Devices
Recent clearances: D.N.E. External Fixation System, S.E.A.L. FRACTURE FUSION TUBE, DNE EXTERNAL FIXATION SYSTEM
3
Total
3
Cleared
0
Denied
Dne, LLC has 3 FDA 510(k) cleared medical devices. Based in Round Rock, US.
Historical record: 3 cleared submissions from 2012 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Dne, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Memphis Regulatory Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dne, LLC
3 devices