
Venocare, Inc.
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Navi Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG) is an FDA 510(k)-cleared medical device (K244047) manufactured by Venocare, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 22, 2025. Regulation: 8.