Ortho8, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2022-06-03
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K220761 | CIRCUL8 Connect DVT Prevention Device | JOW | 2022-06-03 | View |
| 510(k) | K212731 | Circul8 Pro | JOW | 2021-11-15 | View |
| 510(k) | K211235 | CIRCUL8 Luxe DVT Prevention Device | JOW | 2021-09-08 | View |
No matching devices.