# Dixi Medical

- Location (FDA's records): Chaudefontaine, FR
- FDA decisions: 3 (2017–2021): 3 510(k) clearances
- Product codes: GZL (2), GYC (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 9 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ad-Tech Medical Instrument Corp: 3 (https://510kreport.com/company/ad-tech-medical-instrument)
- Pmt Corp.: 1 (https://510kreport.com/company/pmt)
- Radionics, A Division of Tyco Healthcare Group LP: 1 (https://510kreport.com/company/radionics-a-division-of-tyco-healthcare-group)

## Firms that cite its devices most
- Sensomedical Labs, Ltd.: 1 (https://510kreport.com/company/sensomedical-labs)
- Beijing Sinovation Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/beijing-sinovation-medical-technology)
- Neuroone Medical Technologies Corp.: 1 (https://510kreport.com/company/neuroone-medical-technologies)

## Its most-cited devices
- K170959: DIXI Medical Microdeep Depth Electrode (2017), cited by 3

## Recent decisions
- K202087: DIXI Medical Microdeep Micro-Macro Depth Electrodes (Nov 18, 2021)
- K201931: Dixi Medical Intraoperative Subdural Electrodes (Strips and Grids) (Oct 2, 2021)
- K170959: DIXI Medical Microdeep Depth Electrode (Nov 24, 2017)

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