Verge Medical, Inc.
FLASH Flex Aorto-Ostial Angioplasty System
SKU K254022UPC LOX
In Stock
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IIFDA 510(k) Cleared (K254022)
1
Free shipping on orders over $99 · 30-day returns
Verge Medical, Inc.
Free shipping on orders over $99 · 30-day returns
FLASH Flex Aorto-Ostial Angioplasty System is an FDA 510(k)-cleared medical device (K254022) manufactured by Verge Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 1, 2026. Regulation: 8.
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