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Apollo Endosurgery, Inc.
Free shipping on orders over $99 · 30-day returns
APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE SX System is an FDA 510(k)-cleared medical device (DEN210045) 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 July 11, 2022. Regulation: 8.

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