[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]

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

NCT06830057 ·Status: WITHHELD

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

NCT03805074 ·Status: WITHHELD

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

NCT02800057 ·Status: WITHHELD

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

NCT01950767 ·Status: WITHHELD

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

NCT01883557 ·Status: WITHHELD

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

NCT07225075 ·Status: WITHHELD

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

NCT07215377 ·Status: WITHHELD

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

NCT01795807 ·Status: WITHHELD

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

NCT02280577 ·Status: WITHHELD

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

NCT00850109 ·Status: WITHHELD

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

NCT06819072 ·Status: WITHHELD

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

NCT04558047 ·Status: WITHHELD

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

NCT06080867 ·Status: WITHHELD

Clinical Trial of a Hydrophilic EMV Toric Lens RAO210T in the Correction of Aphakia and Corneal Astigmatism

NCT05985304 ·Status: COMPLETED ·Phase: NA

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

NCT00587509 ·Status: WITHHELD

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

NCT05387772 ·Status: WITHHELD

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

NCT05097859 ·Status: WITHHELD

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

NCT05084144 ·Status: WITHHELD

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

NCT07068997 ·Status: WITHHELD

OXINIUM◊ DH Total Hip Arthroplasty Pivotal Study

NCT02353377 ·Status: ACTIVE_NOT_RECRUITING

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

NCT00900705 ·Status: WITHHELD

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

NCT06819085 ·Status: WITHHELD

Effect of the Amplifi™ Vein Dilation System on Outflow Vein Dilation and AV Fistula Maturation (AMPLIFI-1)

NCT07211035 ·Status: RECRUITING ·Phase: NA

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

NCT00578487 ·Status: WITHHELD