Overture Resurfacing, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Overture Resurfacing, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Overture Orthopaedics Patellofemoral System, Uni Knee Resurfacing System
2
Total
2
Cleared
0
Denied
Overture Resurfacing, Inc. has 2 FDA 510(k) cleared medical devices. Based in New York, US.
Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Overture Resurfacing, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Cor Medical Ventures, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Overture Resurfacing, Inc.
2 devices