# Mri Manufacturing and Research, Inc.

- Location (FDA's records): Tuscon, AZ
- FDA decisions: 3 (1996–2009): 3 510(k) clearances
- Product codes: EZL (2), KNT (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 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
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)
- Abco Dealers, Inc.: 1 (https://510kreport.com/company/abco-dealers)

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

## Its most-cited devices
- K083685: Endovive Low Profile Replacement Gastrostomy Tube, Model 82XX, 8283, 8284, 8285 (2009), cited by 1

## Recent decisions
- K083685: Endovive Low Profile Replacement Gastrostomy Tube, Model 82XX, 8283, 8284, 8285 (Jun 25, 2009)
- K982970: Mri's All Silicone Irrigation 3-Way Foley Catheter (Oct 28, 1998)
- K944676: Mri's All  Silicone Foley Catheter (Apr 5, 1996)

Source page: https://510kreport.com/company/mri-manufacturing-and-research