FDA 510(k) Applications Submitted by Ortho8 Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K212731 | 08/30/2021 | Circul8 Pro | Ortho8 Inc. |
| K211235 | 04/26/2021 | CIRCUL8 Luxe DVT Prevention Device | Ortho8 Inc. |
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