MolecuLight, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories1
Latest FDA decision2022-05-18
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K213840 | MolecuLight I:X | QJF | 2022-05-18 | View |
| 510(k) | K211901 | MolecuLightDX | QJF | 2021-07-21 | View |
| 510(k) | K210882 | MolecuLight I:X | QJF | 2021-06-22 | View |
| 510(k) | K191371 | MolecuLight i:X | QJF | 2019-12-04 | View |
No matching devices.
Related Clinical Trials
NCT04207099Comparing Wound Area Reduction of Non-healing DFUs Using MolecuLight i:X Versus Standard of CareCOMPLETEDNCT05196880Biofilm Correlation and ValidationCOMPLETEDNCT06682923MolecuLightDX Measurement Feature Clinical ValidationCOMPLETEDNCT07646938MolecuLight All-in-One Oxygenation Clinical UtilityCOMPLETED