
Boehringer Laboratories, LLC
Free shipping on orders over $99 · 30-day returns
ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340) is an FDA 510(k)-cleared medical device (K234033) manufactured by Boehringer Laboratories, LLC. 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 May 5, 2024. Regulation: 8.