# Medx, Inc.

- Location (FDA's records): Arlington Heights, IL
- FDA decisions: 11 (1987–2008): 11 510(k) clearances
- Names in FDA's records: Medx, Inc. (8); Medx Corp. (3)
- Product codes: IYX (4), KPS (3), IKK (3), IZH (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 2 (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 whose devices it cites most
- Sitco, Inc.: 2 (https://510kreport.com/company/sitco)
- Danish Diagnostic Development A/S: 1 (https://510kreport.com/company/danish-diagnostic-development-a-s)
- Inter Medical Medizintechnik GmbH: 1 (https://510kreport.com/company/inter-medical-medizintechnik)
- General Electric Co.: 1 (https://510kreport.com/company/general-electric)

## Firms that cite its devices most
- Scandia Corporation: 1 (https://510kreport.com/company/scandia)
- Giotto USA, LLC: 1 (https://510kreport.com/company/giotto-usa)

## Its most-cited devices
- K012953: Giotto Image (2001), cited by 1
- K073456: T-Quest System (2007), cited by 1

## Recent decisions
- K082581: C-Quest (Nov 14, 2008)
- K073456: T-Quest System (Dec 20, 2007)
- K041840: Medx Nuquest - Intecam Spect 37-75 System (Aug 20, 2004)
- K012953: Giotto Image (Nov 30, 2001)
- K993893: Medx Intecam Interface (Feb 10, 2000)
- K911666: Medx Machine (Jul 3, 1991)
- K896553: Medx Cervical Extension Test & Rehab Machine (Jan 2, 1990)
- K895236: Medx Rehabilitation Machine (Sep 14, 1989)

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