OCS™ Liver

Currently being evaluated in clinical trials for utilized and unutilized donor livers

Actively Enrolling in US FDA Pivotal Trial for Extended Criteria and DCD Donor Livers

A prospective, pivotal, randomized trial to evaluate the effectiveness of the OCS Liver to preserve and assess donor livers intended for transplantation.

  • Incidence of Early Liver Allograft Dysfunction (EAD) [ Time Frame: 7 days ]
  • Incidence of liver graft related Serious Adverse Events (SAEs) [ Time Frame: 30 days ]

The OCS is designed to enable surgeons to transplant more organs from the available donor pool and to achieve better procedural outcomes.

ClinicalTrials.gov Identifier: NCT02522871

Locate an OCS Liver Trial Center

The OCS Liver System is undergoing clinical trials in the US. The OCS Liver device is an investigational device limited by federal law to investigational use in the US.

Massachusetts General Hospital

Main Campus
55 Fruit Street
Boston, MA 02114

(617) 726-2000

Houston Methodist Hospital

6565 Fannin St
Houston, TX 77030

(713) 790-3311

Henry Ford Hospital

2799 W Grand Blvd
Detroit, MI 48202

(313) 916-2600

UT Southwestern Medical Center

5323 Harry Hines Blvd
Dallas, TX 75390

(214) 648-3111

University of Virginia HSC

1189-1221 Lee St
Charlottesville, VA 22903

(800) 251-3627

MCV Hospitals

1250 East Marshall Street 
Richmond, VA 23298

(804) 828-4104

Emory University Hospital

Johns Hopkins Hospital

1800 Orleans St
Baltimore, MD 21287

(410) 955-5000

University of Minnesota Medical Center

909 Fulton St. SE
Minneapolis, MN 55455

(612) 273-8383

University of Washington Medical Center

9725 3rd Ave NE #400
Seattle, WA 98115

(206) 598-3300

University of CA San Francisco Medical Center

505 Parnassus Ave
San Francisco, CA 94143

(415) 353-1664

Ohio State University Medical Center

410 W 10th Ave
Columbus, OH 43210

(614) 293-8000

The OCS Lung, OCS Heart and OCS Liver are all CE marked devices.
The OCS Lung is an FDA-approved device for utilized donor lungs. The OCS Heart and OCS Liver devices are investigational devices and, therefore, are limited by federal law to investigational use in the US.

ONLY
multi-organ platform

SUBSTANTIAL
body of clinical evidence