[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]

NCT03236519 ·Status: WITHHELD

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

NCT02599519 ·Status: WITHHELD

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

NCT06039813 ·Status: WITHHELD

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

NCT04065659 ·Status: WITHHELD

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

NCT06156839 ·Status: WITHHELD

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

NCT05980039 ·Status: WITHHELD

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

NCT06113159 ·Status: WITHHELD

Wave Crossover ECP Study for Simplified Therapy

NCT06571370 ·Status: COMPLETED ·Phase: NA

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

NCT01365689 ·Status: WITHHELD

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

NCT06008132 ·Status: WITHHELD

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

NCT05618639 ·Status: WITHHELD

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

NCT06546501 ·Status: WITHHELD

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

NCT05619549 ·Status: WITHHELD

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

NCT05085691 ·Status: WITHHELD

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

NCT00961519 ·Status: WITHHELD

Evaluation of Dynavisc in Pain Reduction Following Revision Surgery for Persistent or Recurrent Carpal Tunnel Syndrome

NCT06593977 ·Status: RECRUITING ·Phase: NA

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

NCT06253143 ·Status: WITHHELD

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

NCT00591513 ·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]

NCT06617598 ·Status: WITHHELD

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

NCT06857591 ·Status: WITHHELD

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

NCT02631213 ·Status: WITHHELD

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

NCT04616599 ·Status: WITHHELD

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

NCT06592040 ·Status: WITHHELD

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

NCT04189913 ·Status: WITHHELD