Ignite Orthopedics, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ignite Orthopedics, LLC - FDA 510(k) Cleared Devices
Recent clearances: Ignite Stemless Anatomic Shoulder System, Ignite Anatomic Shoulder System
2
Total
2
Cleared
0
Denied
Ignite Orthopedics, LLC has 2 FDA 510(k) cleared medical devices. Based in Winona Lake, US.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Ignite Orthopedics, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ignite Orthopedics, LLC
2 devices