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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 / K261093

510(k) cleared

DIAFIL

DiaDent Group International · Jun 2, 2026 · K261093

FDA cleared the DIAFIL from DiaDent Group International on Jun 2, 2026 under K261093, a traditional 510(k). The device falls under product code EBF, Material, Tooth Shade, Resin, regulated at 21 CFR 872.3690 as a Class 2 device. The review panel was Dental.

FDA logged the submission as received on Apr 2, 2026. The decision came 61 days later, inside the 90 FDA-day goal for a 510(k).

DiaDent Group International has 3 other decisions in the tracker over the last 12 months: K261166 (DIA-CEM), K261071 (DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g)), K254112 (Dia-X Sil Bite).

Questions & Answers

What did FDA clear under K261093?

K261093 is the FDA 510(k) for DIAFIL, submitted by DiaDent Group International. FDA's decision date was Jun 2, 2026, under product code EBF (Material, Tooth Shade, Resin).

Who makes the DIAFIL?

DiaDent Group International, based in Cheongju-Si, is the applicant of record for K261093.

How long did the K261093 review take?

FDA received the submission on Apr 2, 2026 and issued its decision on Jun 2, 2026, 61 days later.

← All decisions in June 2026

Sources