Ignite Orthomotion is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ignite Orthomotion - FDA 510(k) Cleared Devices
Recent clearances: Achieve Partial Knee System - Porous Coated CoCrMo Femoral Component, ACHIEVE Partial Knee System
2
Total
2
Cleared
0
Denied
Ignite Orthomotion has 2 FDA 510(k) cleared medical devices. Based in Winona Lake, US.
Latest FDA clearance: Sep 2025. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Ignite Orthomotion Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ignite Orthomotion
2 devices