COMPANY
FDA-cleared device company
Location: Campbell, CA · source · Oct 14, 2026
Profile checked Oct 10, 2026
Timeline
- FDA FDA 510(k) clearance: FLASH Flex Aorto-Ostial Angioplasty System — K254022, Apr 2, 2026. Applicant at approval: Verge Medical, Inc. source ↗
- FDA FDA 510(k) clearance: RoVo Mechanical Thrombectomy System — K253730, Jan 21, 2026. Applicant at approval: Verge Medical, Inc. source ↗
FDA records (last 2 years)
- FDA 510(k) clearance: FLASH Flex Aorto-Ostial Angioplasty System — K254022, Apr 2, 2026. Applicant at approval: Verge Medical, Inc. source ↗
- FDA 510(k) clearance: RoVo Mechanical Thrombectomy System — K253730, Jan 21, 2026. Applicant at approval: Verge Medical, Inc. source ↗
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