
Reshape Lifesciences
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Gastrointestinal Boundary Identifier (GIBI HD) is an FDA 510(k)-cleared medical device (K221898) manufactured by Reshape Lifesciences. 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 27, 2022. Regulation: 8.