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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 / June 2026 / K253115

510(k) cleared

LARS ACJ

Movmedix S.A.S. · Jun 10, 2026 · K253115

FDA cleared the LARS ACJ from Movmedix S.A.S. on Jun 10, 2026 under K253115, a traditional 510(k). The device falls under product code HTN, Washer, Bolt Nut, regulated at 21 CFR 888.3030 as a Class 2 device. The review panel was Orthopedic.

FDA logged the submission as received on Sep 24, 2025. The decision came 259 days later, longer than the 90 FDA-day review goal, which usually means at least one additional information request.

This is the only decision on file for Movmedix S.A.S. in the last 12 months of the tracker.

Questions & Answers

What did FDA clear under K253115?

K253115 is the FDA 510(k) for LARS ACJ, submitted by Movmedix S.A.S.. FDA's decision date was Jun 10, 2026, under product code HTN (Washer, Bolt Nut).

Who makes the LARS ACJ?

Movmedix S.A.S., based in Arc-Sur-Tille, is the applicant of record for K253115.

How long did the K253115 review take?

FDA received the submission on Sep 24, 2025 and issued its decision on Jun 10, 2026, 259 days later.

← All decisions in June 2026