ViOptix, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250519 | Lap.Ox™ Laparoscopic Tissue Oximeter | MUD | 2025-06-26 | View |
| 510(k) | K233488 | Intra.Ox™ 2.0 Handheld Tissue Oximeter | MUD | 2024-02-28 | View |
| 510(k) | K221010 | Intra.Ox 2.0 Handheld Tissue Oximeter | MUD | 2022-05-03 | View |
| 510(k) | K191676 | Intra.Ox 2.0 Handheld Tissue Oximeter | MUD | 2019-09-16 | View |
| 510(k) | K163472 | Intra.Ox Handheld Tissue Oximeter | MUD | 2017-11-16 | View |
| 510(k) | K090679 | VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM | MVR | 2009-04-17 | View |
| 510(k) | K042657 | VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-2 | MUD | 2005-01-10 | View |
No matching devices.
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