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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 / K261251

510(k) cleared

Snorbliss® Anti-Snoring Device

Endeavor Commerce, LLC · Jun 11, 2026 · K261251

FDA cleared the Snorbliss® Anti-Snoring Device from Endeavor Commerce, LLC on Jun 11, 2026 under K261251, a traditional 510(k). The device falls under product code LRK, Device, Anti-Snoring, regulated at 21 CFR 872.5570 as a Class 2 device. The review panel was Dental.

FDA logged the submission as received on Apr 16, 2026. The decision came 56 days later, inside the 90 FDA-day goal for a 510(k).

This is the only decision on file for Endeavor Commerce, LLC in the last 12 months of the tracker.

Questions & Answers

What did FDA clear under K261251?

K261251 is the FDA 510(k) for Snorbliss® Anti-Snoring Device, submitted by Endeavor Commerce, LLC. FDA's decision date was Jun 11, 2026, under product code LRK (Device, Anti-Snoring).

Who makes the Snorbliss® Anti-Snoring Device?

Endeavor Commerce, LLC, based in Sheridan, WY, is the applicant of record for K261251.

How long did the K261251 review take?

FDA received the submission on Apr 16, 2026 and issued its decision on Jun 11, 2026, 56 days later.

← All decisions in June 2026