Verge Medical, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest Approval2026-04-02
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K254022 | FLASH Flex Aorto-Ostial Angioplasty System | LOX | 2026-04-02 | View |
| 510(k) | K253730 | RoVo Mechanical Thrombectomy System | QEW | 2026-01-21 | View |
No matching devices.