VereSee Optical Veres Needle and Endoscopic Camera

VereSee Optical Veres Needle and Endoscopic Camera is an FDA 510(k)-cleared medical device (K252640) manufactured by Freyja Healthcare, 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 October 19, 2025. Regulation: 8.