| Primary Device ID | 00855574003083 |
| NIH Device Record Key | 1db953ae-dc36-4c16-8cc8-8dd53616ca5a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KXL System |
| Version Model Number | 110-02724 |
| Company DUNS | 007274362 |
| Company Name | AVEDRO, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | true |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |