[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]

NCT06613672 ·Status: WITHHELD

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

NCT07076173 ·Status: WITHHELD

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

NCT00676078 ·Status: WITHHELD

Investigation on a New Power Knee Firmware Update on Gait and Daily Life Activities for Transfemoral Amputees

NCT06620861 ·Status: TERMINATED ·Phase: NA

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

NCT01906736 ·Status: WITHHELD

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

NCT06753760 ·Status: WITHHELD

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

NCT03132363 ·Status: WITHHELD

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

NCT06601166 ·Status: WITHHELD

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

NCT06100861 ·Status: WITHHELD

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

NCT01016236 ·Status: WITHHELD

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

NCT06762340 ·Status: WITHHELD

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

NCT06709261 ·Status: WITHHELD

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

NCT03696316 ·Status: WITHHELD

The STTAR-US Study: A Pivotal Study of Transcatheter Tricuspid Annular Repair in the US

NCT06700239 ·Status: NOT_YET_RECRUITING ·Phase: NA

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

NCT01607606 ·Status: WITHHELD

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

NCT00767910 ·Status: WITHHELD

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

NCT06138665 ·Status: WITHHELD

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

NCT00587613 ·Status: WITHHELD

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

NCT00760643 ·Status: WITHHELD

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

NCT04616833 ·Status: WITHHELD

A Randomized, Active-Controlled, Double-Masked, Crossover Study to Evaluate the Clinical Performance of Deseyne (Vifilcon C) Daily Disposable Soft Contact Lens for Presbyopia Extended Depth of Focus (EDOF)

NCT06698731 ·Status: COMPLETED ·Phase: NA

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

NCT03663010 ·Status: WITHHELD

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

NCT00670137 ·Status: WITHHELD

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

NCT05557630 ·Status: WITHHELD

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

NCT01697813 ·Status: WITHHELD