Ingenium Spine is one of 16144 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ingenium Spine - FDA 510(k) Cleared Devices
Recent clearances: Ingenix Spinal System, Arisstos™ Spinal System
2
Total
2
Cleared
0
Denied
Ingenium Spine has 2 FDA 510(k) cleared medical devices. Based in Phoenix, US.
Latest FDA clearance: Jun 2024. Active since 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Ingenium Spine Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mrc-X, LLC and MRC Global, LLC.
FDA 510(k) Regulatory Record - Ingenium Spine
2 devices