Avanti Orthopaedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avanti Orthopaedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Avanti Orthopaedics 2.2mm and 2.7mm Cannulated Screws, Avanti Orthopaedics 3.2mm and 4.0mm Cannulated Screws, Avanti Orthopaedics Ulnar Shortening System, Avanti Distal Radius and Forearm System
3
Total
3
Cleared
0
Denied
Avanti Orthopaedics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Last cleared in 2022. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Avanti Orthopaedics, Inc. 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, Inc.
3 devices