COMPANY
Carl Zeiss Meditec
FDA-cleared device company Clinical Phase 3
Timeline
- Trial start Phase 4: Toric Performance And Constant Evaluation source ↗
- Trial start —: Evaluation of Glistening, Visual Outcomes and General Safety 24 Months Post-IOL Implantation source ↗
- Trial start Not phased (device or behavioral study): Extended Depth of Focus (EDF) Intraocular Lens (IOL) Versus Monofocal Intracoular Lens (IOL) source ↗
- Trial start —: Evaluation of Cataract Surgery Outcomes in Patients With Prior Laser Vision Correction Implanted With the CT LUCIA Lens source ↗
- Raise Private equity round — Series A: amount not published, announced May 28, 2025. Source: company's own press page. source ↗
- Partnership Partnership / licensing announced May 13, 2025. Source: company's own press page. source ↗
- Trial start —: Evaluation of Refractive Outcomes in Patients Undergoing PRESBYOND Using the MEL90 Excimer Laser source ↗
- Trial start Not phased (device or behavioral study): AT ELANA 841P Posterior Chamber Intraocular Lens for Correction of Aphakia Following Cataract Removal source ↗
- Trial start Phase 4: Evaluation of a Monofocal Intraocular Lens source ↗
- Trial start Not phased (device or behavioral study): Visual Performance of Patients Implanted With a Multifocal IOL source ↗
- Trial start —: Safety and Performance of Hydrophobic and Hydrophilic Intraocular Lenses After Bilateral Cataract Surgery source ↗
- Trial start Not phased (device or behavioral study): Study to Confirm Safety and Performance of a New Multifocal IOL source ↗
- Trial start Not phased (device or behavioral study): 621 Real World Study source ↗
- Trial start Not phased (device or behavioral study): A Prospective Multicenter Study To Assess The Clinical Outcomes Of Current Phacoemulsification Approach To Cataract Extraction Versus The Micor System Device source ↗
- Trial start Not phased (device or behavioral study): Feasibility Investigation of Biometry and Tomography Measurements in a Heterogeneous Patient Cohort source ↗
- Trial start —: Post-approval Study of New Enrolment Patients Undergoing Bilateral Treatment With the VisuMax SMILE Procedure source ↗
- Trial start Not phased (device or behavioral study): Study to Optimize the IOL Constant of a New Multifocal Intraocular Lens source ↗
- Trial start —: Evaluation of a Spherical Hydrophilic Acrylic Intraocular Lens source ↗
- Trial start —: Safety and Effectiveness of an Hydrophilic Acrylic Intraocular Lens source ↗
- Trial start —: PMCF Study on SMILE Treatment of Myopia With and Without Astigmatism source ↗
- Trial start Not phased (device or behavioral study): Prospective Evaluation of an Hydrophilic Acrylic Intraocular Lens source ↗
- Trial start Not phased (device or behavioral study): Visual Perception After Virtual Implantation source ↗
- Trial start —: Evaluation of an Hydrophilic Acrylic Intraocular Lens source ↗
- Trial start —: Study on Visual Performance of a Monofocal Intraocular Lens source ↗
- Trial start Not phased (device or behavioral study): Assessment of Low Energy Lens Fragmentation Cataract Extraction in Patients Undergoing Cataract Surgery source ↗
Upcoming milestones
- Feb 28, 2028 (ESTIMATED) · Phase 4 · Toric Performance And Constant Evaluation · NCT07471295
Funding
Clinical trials (lead sponsor) Showing 50 of 54
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT07297719 | Evaluation of Glistening, Visual Outcomes and General Safety 24 Months Post-IOL Implantation | Not listed | Completed | Dec 25, 2025 | Dec 31, 2025 (actual) |
| NCT07092020 | Extended Depth of Focus (EDF) Intraocular Lens (IOL) Versus Monofocal Intracoular Lens (IOL) | Not phased (device or behavioral study) | Completed | Oct 1, 2025 | Jul 27, 2026 (actual) |
| NCT06264232 | AT ELANA 841P Posterior Chamber Intraocular Lens for Correction of Aphakia Following Cataract Removal | Not phased (device or behavioral study) | Completed | Jul 12, 2024 | Nov 3, 2025 (actual) |
| NCT06428955 | Evaluation of a Monofocal Intraocular Lens | Phase 4 | Completed | Jun 6, 2024 | Feb 26, 2026 (actual) |
| NCT06111222 | Visual Performance of Patients Implanted With a Multifocal IOL | Not phased (device or behavioral study) | Completed | Oct 31, 2023 | Jan 13, 2026 (actual) |
| NCT07471295 | Toric Performance And Constant Evaluation | Phase 4 | Recruiting | Jul 13, 2026 | Feb 28, 2028 (estimated) |
| NCT05646004 | 621 Real World Study | Not phased (device or behavioral study) | Completed | Jan 9, 2023 | Nov 27, 2023 (actual) |
| NCT05729477 | A Prospective Multicenter Study To Assess The Clinical Outcomes Of Current Phacoemulsification Approach To Cataract Extraction Versus The Micor System Device | Not phased (device or behavioral study) | Terminated | Dec 6, 2022 | Nov 30, 2025 (actual) |
| NCT01638390 | Use of the VisuMax™ Femtosecond Laser | Phase 1 | Completed | 2012-07 | 2016-04 (actual) |
| NCT05740293 | Post-approval Study of New Enrolment Patients Undergoing Bilateral Treatment With the VisuMax SMILE Procedure | Not listed | Completed | Apr 5, 2022 | Sep 1, 2024 (actual) |
| NCT07084545 | Evaluation of Cataract Surgery Outcomes in Patients With Prior Laser Vision Correction Implanted With the CT LUCIA Lens | Not listed | Recruiting | 2025-07 | 2026-07 (estimated) |
| NCT06960785 | Evaluation of Refractive Outcomes in Patients Undergoing PRESBYOND Using the MEL90 Excimer Laser | Not listed | Not yet recruiting | 2025-05 | 2026-01 (estimated) |
| NCT04519814 | Safety and Effectiveness of VISULAS Green Selective Laser Trabeculoplasty (SLT) | Not phased (device or behavioral study) | Completed | Jun 30, 2020 | Nov 23, 2021 (actual) |
| NCT06247683 | Study to Confirm Safety and Performance of a New Multifocal IOL | Not phased (device or behavioral study) | Completed | Mar 13, 2023 | Mar 26, 2024 (actual) |
| NCT04747834 | Assessment of Low Energy Lens Fragmentation Cataract Extraction in Patients Undergoing Cataract Surgery | Not phased (device or behavioral study) | Completed | Jan 6, 2021 | Jan 24, 2022 (actual) |
| NCT06192901 | Safety and Performance of Hydrophobic and Hydrophilic Intraocular Lenses After Bilateral Cataract Surgery | Not listed | Completed | Sep 18, 2023 | Sep 22, 2023 (actual) |
| NCT04884672 | PMCF Study on SMILE Treatment of Myopia With and Without Astigmatism | Not listed | Completed | Jul 9, 2021 | Mar 25, 2023 (actual) |
| NCT04252716 | VISPER: Randomised Comparison of Two OVDs in Cataract Surgery | Not listed | Completed | Sep 24, 2020 | Nov 24, 2021 (actual) |
| NCT04907500 | Prospective Evaluation of an Hydrophilic Acrylic Intraocular Lens | Not phased (device or behavioral study) | Completed | Jun 22, 2021 | Aug 6, 2022 (actual) |
| NCT03839420 | To Compare Early Rotation of Two Extended Depth of Focus Intraocular Lenses | Not phased (device or behavioral study) | Completed | Jul 8, 2019 | Oct 4, 2020 (actual) |
| NCT05201027 | Study to Optimize the IOL Constant of a New Multifocal Intraocular Lens | Not phased (device or behavioral study) | Terminated | Jan 28, 2022 | Jul 27, 2022 (actual) |
| NCT04545671 | Evaluation of a Trifocal Lens | Not listed | Completed | Nov 1, 2020 | Mar 16, 2022 (actual) |
| NCT05462067 | Combined EDOF / Trifocal | Not phased (device or behavioral study) | Completed | Mar 14, 2019 | Nov 20, 2020 (actual) |
| NCT05458661 | Feasibility Investigation of Biometry and Tomography Measurements in a Heterogeneous Patient Cohort | Not phased (device or behavioral study) | Unknown status (ClinicalTrials.gov) | 2022-08 | 2023-03 (estimated) |
| NCT04789538 | Safety and Effectiveness of an Hydrophilic Acrylic Intraocular Lens | Not listed | Completed | Aug 31, 2021 | Apr 1, 2022 (actual) |
| NCT04793789 | Evaluation of an Hydrophilic Acrylic Intraocular Lens | Not listed | Completed | Apr 27, 2021 | Jan 24, 2022 (actual) |
| NCT04998409 | Evaluation of a Spherical Hydrophilic Acrylic Intraocular Lens | Not listed | Completed | Sep 24, 2021 | Apr 22, 2022 (actual) |
| NCT04967612 | Visual Perception After Virtual Implantation | Not phased (device or behavioral study) | Completed | May 10, 2021 | Aug 19, 2021 (actual) |
| NCT04740788 | Study on Visual Performance of a Monofocal Intraocular Lens | Not listed | Completed | Feb 19, 2021 | May 18, 2021 (actual) |
| NCT04037631 | Compare Visual Outcomes Using a New Diagnostic Device | Not listed | Terminated | Jul 20, 2017 | May 1, 2020 (actual) |
| NCT02430428 | Correction of Myopia Wtih or Without Astigmatism Using the VisuMax™ Femtosecond Laser | Not phased (device or behavioral study) | Completed | 2015-03 | 2017-10 (actual) |
| NCT03172351 | EDoF IOLs vs Monofocal IOL | Not phased (device or behavioral study) | Completed | May 24, 2017 | Jan 1, 2019 (actual) |
| NCT03790592 | Visual Outcomes After Presbyopic Lens Exchange | Not phased (device or behavioral study) | Completed | May 14, 2019 | Dec 9, 2019 (actual) |
| NCT03431571 | Use of the VisuMax Femtosecond Laser Lenticule Removal Procedure for the Correction of Hyperopia | Not phased (device or behavioral study) | Unknown status (ClinicalTrials.gov) | Jul 5, 2017 | Dec 31, 2020 (estimated) |
| NCT04036149 | To Compare Postoperative Horizontal Position Stability of the CT LUCIA 611P and the CT ASPHINA 409MP | Not phased (device or behavioral study) | Completed | Mar 14, 2017 | Jul 20, 2018 (actual) |
| NCT02990689 | Clinical Study to Evaluate the Visual Performance of Three Multifocal IOLs | Not phased (device or behavioral study) | Completed | 2012-03 | 2015-04 (actual) |
| NCT00761826 | Study of the MEL 80 Excimer Laser Using LASIK in the Treatment of Mixed Astigmatism | Not phased (device or behavioral study) | Completed | 2007-01 | 2008-12 (actual) |
| NCT00762541 | Study of the MEL 80 Excimer Laser Using LASIK in the Treatment of Moderate to High Myopia | Not phased (device or behavioral study) | Completed | 2006-10 | 2008-07 (actual) |
| NCT03145116 | Clinical Safety and Efficacy of CT ASPHINA 509 Lenses | Not phased (device or behavioral study) | Terminated | Sep 22, 2017 | Feb 5, 2018 (actual) |
| NCT03145103 | Clinical Safety and Efficacy of Hydrophilic Acrylic Intraocular Lenses | Not phased (device or behavioral study) | Completed | Aug 7, 2017 | Jun 26, 2018 (actual) |
| NCT03518775 | Repeatability and Reproducibility of the IOLMaster 700 Vers 1.70 and Agreement With IOLMaster 700 Vers. 1.50 and Pentacam | Not listed | Completed | Mar 16, 2018 | Apr 20, 2018 (actual) |
| NCT02985723 | Visual Outcome, Cylinder Correction and Patient Satisfaction After Implantation of AT LISA Tri Toric 939MP Intraocular Lenses | Not phased (device or behavioral study) | Completed | 2013-03 | 2016-06 (actual) |
| NCT02903927 | Clinical Trial to Evaluate the Visual Performance of Two Monofocal Intraocular Lenses | Not phased (device or behavioral study) | Completed | May 20, 2014 | Jun 6, 2016 (actual) |
| NCT01731743 | Evaluation of Visual Acuity and Patient Satisfaction With AT LISA TRI 839MP Intraocular Lenses | Not phased (device or behavioral study) | Completed | 2012-01 | 2013-07 (actual) |
| NCT02708082 | Glaucoma HFA / OCT Specificity Study | Not listed | Unknown status (ClinicalTrials.gov) | 2016-03 | 2016-08 (estimated) |
| NCT00396188 | Screening Aid to Identify Corneas That May Have Pathologies or Other Conditions | Not listed | Completed | 2007-02 | 2008-02 (actual) |
| NCT01272076 | Cirrus HD-OCT Measurement of Area of Increased Light Penetration Under the Retinal Pigment Epithelium (RPE) | Not listed | Completed | 2011-01 | 2011-02 (actual) |
| NCT00876278 | Night Driving Pilot | Phase 4 | Withdrawn | 2009-06 | 2009-10 (estimated) |
| NCT01890174 | Repeatability and Reproducibility of Cirrus HD-OCT Macular Retinal Pigment Epithelium Elevation | Not listed | Completed | 2011-02 | 2011-06 (actual) |
| NCT01890187 | Repeatability and Reproducibility of Cirrus HD-OCT Measurements of Illumination Areas Under the Retinal Pigment Epithelium | Not listed | Completed | 2010-11 | 2011-02 (actual) |