# Expanding Orthopedics, Inc.

- Location (FDA's records): Colorado Springs, CO
- FDA decisions: 3 (2009–2017): 3 510(k) clearances
- Product codes: MAX (2), NKB (1)
- Predicates its devices cite: 9 (1 its own); citations of its devices by later devices: 5 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Coalign Innovations, Inc.: 3 (https://510kreport.com/company/coalign-innovations)
- Kiscomedica S.A.: 2 (https://510kreport.com/company/kiscomedica)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Custom Spine, Inc.: 1 (https://510kreport.com/company/custom-spine)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)

## Firms that cite its devices most
- Life Spine, Inc.: 1 (https://510kreport.com/company/life-spine)
- Innovasis, Inc.: 1 (https://510kreport.com/company/innovasis)
- Innovasive, Inc.: 1 (https://510kreport.com/company/innovasive)
- Spineex, Inc.: 1 (https://510kreport.com/company/spineex)

## Its most-cited devices
- K133813: Flxfit Intervertebral Body Fusion Device (2014), cited by 3
- K171519: FLXfit™ (2017), cited by 2

## Recent decisions
- K171519: FLXfit™ (Sep 15, 2017)
- K133813: Flxfit Intervertebral Body Fusion Device (Jul 15, 2014)
- K083825: Eoi Spinal System (Mar 19, 2009)

Source page: https://510kreport.com/company/expanding-orthopedics