
Stryker Endoscopy
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L12 LED Light Source with AIM is an FDA 510(k)-cleared medical device (K260108) manufactured by Stryker Endoscopy. 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 February 11, 2026. Regulation: 8.