Ingenium Spine is one of 5511 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
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.
510(k) submissions have been managed by MRC Global, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ingenium Spine
2 devices