# Si-Technology, LLC

- Location (FDA's records): Fort Collins, CO
- FDA decisions: 3 (2015–2025): 3 510(k) clearances
- Product codes: OUR (3)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Tenon Medical: 2 (https://510kreport.com/company/tenon-medical)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- SI-BONE, Inc.: 1 (https://510kreport.com/company/si-bone)
- Globus Medical, Inc.: 1 (https://510kreport.com/company/globus-medical)

## Firms that cite its devices most
- Curiteva, Inc.: 1 (https://510kreport.com/company/curiteva)

## Its most-cited devices
- K151462: SI-Technology® SI-Desis® Screws (2015), cited by 2
- K241813: SI-TECHNOLOGY® SI-DESIS® X™ Sacroiliac Joint Fusion System (2024), cited by 1

## Recent decisions
- K251525: SI-TECHNOLOGY® SI-DESIS® X™ Sacroiliac Joint Fusion System (Jun 6, 2025)
- K241813: SI-TECHNOLOGY® SI-DESIS® X™ Sacroiliac Joint Fusion System (Aug 13, 2024)
- K151462: SI-Technology® SI-Desis® Screws (Aug 12, 2015)

Source page: https://510kreport.com/company/si-technology