Conextions Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Conextions Medical - FDA 510(k) Cleared Devices
Recent clearances: CoNextions TR Tendon Repair System, Coronet Soft Tissue Fixation System
2
Total
2
Cleared
0
Denied
Conextions Medical has 2 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Last cleared in 2022. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Conextions Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Conextions Medical
2 devices