# Xeridiem (Formerly Mri)

- Location (FDA's records): Tucson, AZ
- FDA decisions: 2 (2015–2015): 2 510(k) clearances
- Product codes: PIF (2)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 104 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Kimberly-Clark Corp.: 1 (https://510kreport.com/company/kimberly-clark)
- Applied Medical Technologies: 1 (https://510kreport.com/company/applied-medical-technologies)
- Superior Healthcare Group, Inc.: 1 (https://510kreport.com/company/superior-healthcare-group)

## Firms that cite its devices most
- Xeridiem Medical Devices: 1 (https://510kreport.com/company/xeridiem-medical-devices)

## Its most-cited devices
- K142075: BI-Funnel Gastrostomy Feeding Tube, Tri-Funnel Gastrostomy Feeding Tube (2015), cited by 1

## Recent decisions
- K142297: Endo Vive 3S Low Profile Balloon Kit, Endo Vive 3S Bolus Extension Sets, Endo Vive 3S Continuous Extension Sets, Endo Vive 3S Medication Extension Set (Jan 8, 2015)
- K142075: BI-Funnel Gastrostomy Feeding Tube, Tri-Funnel Gastrostomy Feeding Tube (Jan 8, 2015)

Source page: https://510kreport.com/company/xeridiem-formerly-mri