Omniguide, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest Approval2021-01-14
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K203241 | OmniGuide BeamPath OTO-U Fiber | GEX | 2021-01-14 | View |
| 510(k) | K183199 | TRIO Handpiece | GEX | 2019-05-02 | View |
| 510(k) | K180993 | Beacon Advanced CO2 Laser System | GEX | 2018-06-28 | View |
No matching devices.