# Ionics Medical Corp.

- Location (FDA's records): Ether, NC
- FDA decisions: 2 (2000–2008): 2 510(k) clearances
- Product codes: MAX (1), MQP (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 1 (1 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
- Medtronic Sofamor Danek: 2 (https://510kreport.com/company/medtronic-sofamor-danek)
- Nuvasive, Inc.: 1 (https://510kreport.com/company/nuvasive)
- Stryker Spine: 1 (https://510kreport.com/company/stryker-spine)

## Its most-cited devices
- K983667: Ionics Levante Intervertebral Pillar, Expandable (2000), cited by 1

## Recent decisions
- K081673: Dyn-Alif Anterolateral Intervertebral Body Fusion Device (Nov 14, 2008)
- K983667: Ionics Levante Intervertebral Pillar, Expandable (Jul 5, 2000)

Source page: https://510kreport.com/company/ionics-medical