
EvoEndo, Inc.
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EvoEndo Single-Use Endoscopy System is an FDA 510(k)-cleared medical device (K251708) manufactured by EvoEndo, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 9, 2025. Regulation: 8.