# Kiscomedica S.A.

- Location (FDA's records): Round Rock, TX
- FDA decisions: 1 (2008–2008): 1 510(k) clearance
- Product codes: MAX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 13 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Expanding Orthopedics, Inc.: 2 (https://510kreport.com/company/expanding-orthopedics)
- Globus Medical, Inc.: 2 (https://510kreport.com/company/globus-medical)
- Interventional Spine, Inc.: 2 (https://510kreport.com/company/interventional-spine)
- Life Spine, Inc.: 1 (https://510kreport.com/company/life-spine)
- Nanovis, LLC: 1 (https://510kreport.com/company/nanovis)
- Spectrum Spine, LLC: 1 (https://510kreport.com/company/spectrum-spine)
- Wenzel Spine, Inc.: 1 (https://510kreport.com/company/wenzel-spine)
- Thompson Mis, Inc.: 1 (https://510kreport.com/company/thompson-mis)

## Its most-cited devices
- K080537: L-Varlock (2008), cited by 13

## Recent decisions
- K080537: L-Varlock (Jun 30, 2008)

Source page: https://510kreport.com/company/kiscomedica