RightLance Blood Lancing System

K222034 is the FDA 510(k) clearance record for RightLance Blood Lancing System, a class II device, cleared for Beijing Ruicheng Medical Supplies Co., Ltd. on 2022-09-07 under FDA product code QRL (Multiple Use Blood Lancet For Single Patient Use Only). FDA's definition for product code QRL reads: "A multiple use capable blood lancet intended for use on a single patient that is comprised of a single use blade attached to a solid, reusable base that is used to puncture the skin to obtain a drop of blood for diagnostic purposes". FDA records list 2 510(k) clearances for Beijing Ruicheng Medical Supplies Co., Ltd., from 2022-09-07 to 2022-11-29. As of 2026-09-10, FDA records show no recalls naming K222034.