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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 / K260819

510(k) cleared

Any-Com Seal

Mediclus Co., Ltd. · May 1, 2026 · K260819

FDA cleared the Any-Com Seal from Mediclus Co., Ltd. on May 1, 2026 under K260819, a traditional 510(k). The device falls under product code EBC, Sealant, Pit And Fissure, And Conditioner, regulated at 21 CFR 872.3765 as a Class 2 device. The review panel was Dental.

FDA logged the submission as received on Mar 13, 2026. The decision came 49 days later, inside the 90 FDA-day goal for a 510(k).

Mediclus Co., Ltd. has 6 other decisions in the tracker over the last 12 months: K254201 (Any-Cem), K261728 (One-Fil LC), K260485 (Any-Etch), K253797 (One-Stop).

Questions & Answers

What did FDA clear under K260819?

K260819 is the FDA 510(k) for Any-Com Seal, submitted by Mediclus Co., Ltd.. FDA's decision date was May 1, 2026, under product code EBC (Sealant, Pit And Fissure, And Conditioner).

Who makes the Any-Com Seal?

Mediclus Co., Ltd., based in Cheongju-Si, is the applicant of record for K260819.

How long did the K260819 review take?

FDA received the submission on Mar 13, 2026 and issued its decision on May 1, 2026, 49 days later.

← All decisions in May 2026

Sources