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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 / October 2025 / K252384

510(k) cleared

DESS® Dental Smart Solutions

Terrats Medical SL · Oct 23, 2025 · K252384

FDA cleared the DESS® Dental Smart Solutions from Terrats Medical SL on Oct 23, 2025 under K252384, a traditional 510(k). The device falls under product code NHA, Abutment, Implant, Dental, Endosseous, regulated at 21 CFR 872.3630 as a Class 2 device. The review panel was Dental.

FDA logged the submission as received on Jul 31, 2025. The decision came 84 days later, inside the 90 FDA-day goal for a 510(k).

Terrats Medical SL has 3 other decisions in the tracker over the last 12 months: K260564 (DESS Dental Smart Solutions), K253804 (DESS Dental Smart Solutions), K251547 (DESS Dental Smart Solutions).

Questions & Answers

What did FDA clear under K252384?

K252384 is the FDA 510(k) for DESS® Dental Smart Solutions, submitted by Terrats Medical SL. FDA's decision date was Oct 23, 2025, under product code NHA (Abutment, Implant, Dental, Endosseous).

Who makes the DESS® Dental Smart Solutions?

Terrats Medical SL, based in Barberá Del Vallés, is the applicant of record for K252384.

How long did the K252384 review take?

FDA received the submission on Jul 31, 2025 and issued its decision on Oct 23, 2025, 84 days later.

← All decisions in October 2025

Sources