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Verge Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K254022FLASH Flex™ Aorto-Ostial Angioplasty SystemApril 2, 2026
K253730RoVo Mechanical Thrombectomy SystemJanuary 21, 2026