Avanti Orthopaedics, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avanti Orthopaedics, LLC - FDA 510(k) Cleared Devices
Recent clearances: Avanti Distal Elbow ORIF System
1
Total
1
Cleared
0
Denied
Avanti Orthopaedics, LLC has 1 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Avanti Orthopaedics, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Secure BioMed Evaluations as regulatory consultant.
FDA 510(k) Regulatory Record - Avanti Orthopaedics, LLC
1 devices