# Aci, Inc.

- Location (FDA's records): Lakewood, CO
- FDA decisions: 2 (2006–2007): 2 510(k) clearances
- Product codes: GXD (1), EBI (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 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
- Radionics, Inc.: 1 (https://510kreport.com/company/radionics)
- Mercury Medical: 1 (https://510kreport.com/company/mercury-medical)
- Dentsply Intl.: 1 (https://510kreport.com/company/dentsply-intl)

## Firms that cite its devices most
- Bioform Medical, Inc.: 1 (https://510kreport.com/company/bioform-medical)

## Its most-cited devices
- K063753: GFX Nerve Ablation System (2007), cited by 1

## Recent decisions
- K063753: GFX Nerve Ablation System (Jun 20, 2007)
- K061501: Flexo Dental Resin Material (Jul 26, 2006)

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