[Trial of device that is not approved or cleared by the U.S. FDA]

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT03147482 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT01414491 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT07404878 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT01147094 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT04914949 ·Status: WITHHELD

Basic Mobility and Balance Performance of Low Active Transfemoral Prosthesis Users With a Powered Prosthetic Knee

NCT04799145 ·Status: COMPLETED

EVERO Drug-coated Balloon (DCB) Randomized Trial

NCT07144150 ·Status: RECRUITING ·Phase: NA

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT00748917 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT03124745 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT01470079 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT01674400 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT04314947 ·Status: WITHHELD

EndoArt® Implantation in Subjects With Chronic Corneal Edema - US Study

NCT07344168 ·Status: NOT_YET_RECRUITING ·Phase: NA

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT02474784 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT04787484 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT02020447 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT07014995 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT01662479 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT07167407 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT03124719 ·Status: WITHHELD

Agilis RF TSP Early Feasibility Study

NCT07361445 ·Status: RECRUITING ·Phase: NA

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT02474771 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT02474758 ·Status: WITHHELD

[Trial of device that is not approved or cleared by the U.S. FDA]

NCT05084144 ·Status: WITHHELD

Myopia Control With a Innovative Spectacle Lens

NCT05174780 ·Status: COMPLETED ·Phase: NA