| Primary Device ID | 10185571000059 |
| NIH Device Record Key | c96cdbf4-80a5-426a-bec1-92fc9ec5e2fd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Orpyx SI |
| Version Model Number | ORPYXSIV1 - Insoles |
| Company DUNS | 250917031 |
| Company Name | Orpyx |
| 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 | true |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10185571000059 [Primary] |
| IRN | Device, Warning, Overload, External Limb, Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-05-04 |
| Device Publish Date | 2020-04-26 |
| 10185571000127 | The Orpyx® SI sensory insole system is designed to help patients at risk of foot ulceration. Th |
| 10185571000059 | The Orpyx® SI sensory insole system is designed to help patients at risk of foot ulceration. Th |
| 10185571000042 | The Orpyx® SI sensory insole system is designed to help patients at risk of foot ulceration. Th |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ORPYX SI 88555205 not registered Live/Pending |
ORPYX MEDICAL TECHNOLOGIES INC. 2019-07-31 |