# Xeridiem Medical Devices

- Location (FDA's records): Tucson, AZ
- FDA decisions: 3 (2013–2017): 3 510(k) clearances
- Product codes: KNT (2), PIF (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (1 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
- Xeridiem (Formerly Mri): 1 (https://510kreport.com/company/xeridiem-formerly-mri)
- Manufacturing & Research, Inc.: 1 (https://510kreport.com/company/manufacturing-research)
- Mri Manufacturing and Research, Inc.: 1 (https://510kreport.com/company/mri-manufacturing-and-research)

## Firms that cite its devices most
- Xeridiem Medical Devices, A Spectrum Plastics Group Company: 1 (https://510kreport.com/company/xeridiem-medical-devices-a-spectrum-plastics-group)

## Its most-cited devices
- K130611: Entuit Thrive Balloon Retention Gastrostomy Feeding Tube (2013), cited by 1
- K130674: Entuit Thrive LP Balloon Retention Gastrostomy Feeding Tube (2014), cited by 1

## Recent decisions
- K171347: Bi-Funnel and Tri-Funnel Gastrostomy Feeding Tubes with ENFit Connection, Entuit Gastrostomy BR Balloon Retention Feeding Tube with ENFit Connection (Jun 6, 2017)
- K130674: Entuit Thrive LP Balloon Retention Gastrostomy Feeding Tube (Jan 13, 2014)
- K130611: Entuit Thrive Balloon Retention Gastrostomy Feeding Tube (Dec 19, 2013)

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