Si-Technology, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Si-Technology, LLC - FDA 510(k) Cleared Devices
Recent clearances: SI-TECHNOLOGY® SI-DESIS® X™ Sacroiliac Joint Fusion System, SI-TECHNOLOGY® SI-DESIS® X™ Sacroiliac Joint Fusion System
3
Total
3
Cleared
0
Denied
Si-Technology, LLC has 3 FDA 510(k) cleared medical devices. Based in Fort Collins, US.
Latest FDA clearance: Jun 2025. Active since 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Si-Technology, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Secure BioMed Evaluations as regulatory consultant.
FDA 510(k) Regulatory Record - Si-Technology, LLC
3 devices