| Primary Device ID | 00627843933243 |
| NIH Device Record Key | 702b1a4b-92bb-4ba1-84ff-be384c0ac3af |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KneeKG-Exoskeleton |
| Version Model Number | 0 |
| Catalog Number | P-080 |
| Company DUNS | 247640605 |
| Company Name | Emovi Inc |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |