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Elucid raises $55M Series D with FFR-CT 510(k) under FDA review Enovis to buy eCential Robotics for 155 million euros FDA authorizes Vitestro's Aletta, the first autonomous blood-drawing robot, five months after a $70M Series B Renata Medical raises $25M Series D to scale the Minima pediatric stent FDA opens a docket on how to regulate generative AI devices FDA clears Jupiter Endovascular's Vertex thrombectomy system for pulmonary embolism in 89 days FDA clears Wandercraft's Eve, the first self-balancing exoskeleton for home use Meduloc raises $4M Series B to start alpha launch of its nitinol fracture implant FDA sets FY2027 device user fees: $28,653 for a 510(k), $13,785 to register Elucid raises $55M Series D with FFR-CT 510(k) under FDA review Enovis to buy eCential Robotics for 155 million euros FDA authorizes Vitestro's Aletta, the first autonomous blood-drawing robot, five months after a $70M Series B Renata Medical raises $25M Series D to scale the Minima pediatric stent FDA opens a docket on how to regulate generative AI devices FDA clears Jupiter Endovascular's Vertex thrombectomy system for pulmonary embolism in 89 days FDA clears Wandercraft's Eve, the first self-balancing exoskeleton for home use Meduloc raises $4M Series B to start alpha launch of its nitinol fracture implant FDA sets FY2027 device user fees: $28,653 for a 510(k), $13,785 to register

The Tracker / May 2026 / K252776

510(k) cleared

ARIES Anterior Cervical Plate Systems

ZheJiang Decans Medical Devices Co., Ltd. · May 14, 2026 · K252776

FDA cleared the ARIES Anterior Cervical Plate Systems from ZheJiang Decans Medical Devices Co., Ltd. on May 14, 2026 under K252776, a traditional 510(k). The device falls under product code KWQ, Appliance, Fixation, Spinal Intervertebral Body, regulated at 21 CFR 888.3060 as a Class 2 device. The review panel was Orthopedic.

FDA logged the submission as received on Sep 2, 2025. The decision came 254 days later, longer than the 90 FDA-day review goal, which usually means at least one additional information request.

ZheJiang Decans Medical Devices Co., Ltd. has 7 other decisions in the tracker over the last 12 months: K253046 (HERA Interlocking Intramedullary Nailing System), K253195 (TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems), K252930 (AQUA Laminoplasty Systems), K253130 (Dione PEEK Screw System).

Questions & Answers

What did FDA clear under K252776?

K252776 is the FDA 510(k) for ARIES Anterior Cervical Plate Systems, submitted by ZheJiang Decans Medical Devices Co., Ltd.. FDA's decision date was May 14, 2026, under product code KWQ (Appliance, Fixation, Spinal Intervertebral Body).

Who makes the ARIES Anterior Cervical Plate Systems?

ZheJiang Decans Medical Devices Co., Ltd., based in Jiaxing City, is the applicant of record for K252776.

How long did the K252776 review take?

FDA received the submission on Sep 2, 2025 and issued its decision on May 14, 2026, 254 days later.

← All decisions in May 2026