# Neuro Resource Group, Inc.

- Location (FDA's records): Plano, TX
- FDA decisions: 4 (2005–2013): 4 510(k) clearances
- Product codes: GXY (2), GZJ (1), NFO (1)
- Predicates its devices cite: 10 (2 its own); citations of its devices by later devices: 9 (2 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
- Eumedic Limited: 1 (https://510kreport.com/company/eumedic)
- Empi: 1 (https://510kreport.com/company/empi)
- Dynatronics Corp.: 1 (https://510kreport.com/company/dynatronics)
- Covidien: 1 (https://510kreport.com/company/covidien)
- Katecho, Inc.: 1 (https://510kreport.com/company/katecho)
- Classic Medical Products, Inc.: 1 (https://510kreport.com/company/classic-medical-products)
- Salton, Inc.: 1 (https://510kreport.com/company/salton)
- Facemaster of Beverly Hills, Inc.: 1 (https://510kreport.com/company/facemaster-of-beverly-hills)

## Firms that cite its devices most
- Ritm Okb Zao: 2 (https://510kreport.com/company/ritm-okb-zao)
- Med-Lectric Corporation: 2 (https://510kreport.com/company/med-lectric)
- Daka International, Ltd.: 1 (https://510kreport.com/company/daka-international)
- Mid-America Medical Innovations, LLC: 1 (https://510kreport.com/company/mid-america-medical-innovations)
- Avazzia, Inc.: 1 (https://510kreport.com/company/avazzia)

## Its most-cited devices
- K042912: INTERX5000 (2005), cited by 7
- K053626: INTERX500 Flexible Array Electrode (2006), cited by 1
- K070217: Interx 1000/Derma 200 Stimulator for Cosmetic Use (2008), cited by 1

## Recent decisions
- K130816: Interx Sterile Self-Adhesive Dual Electrode (Issde) (Jun 21, 2013)
- K070217: Interx 1000/Derma 200 Stimulator for Cosmetic Use (Apr 4, 2008)
- K053626: INTERX500 Flexible Array Electrode (Mar 29, 2006)
- K042912: INTERX5000 (May 17, 2005)

Source page: https://510kreport.com/company/neuro-resource-group