
Apollo Endosurgery, Inc.
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Apollo ESG NXT System, Apollo REVISE NXT System is an FDA 510(k)-cleared medical device (K232544) manufactured by Apollo Endosurgery, 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 September 17, 2023. Regulation: 8.