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Neurent Medical , Ltd.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2026-06-16
TypeNumberDevice NameCodeDateActions
510(k) K261833 NEUROMARK System (NMK00301)GEI2026-06-16 View
510(k) K250048 NEUROMARK System (NMK00301)GEI2025-05-29 View

Related Clinical Trials

NCT05324397Safety and Efficacy Study of the Neurent Medical NEUROMARK™ System in Subjects With Chronic Rhinitis (CLARITY)COMPLETEDNCT05591989Clinical Evaluation of Safety and Efficacy for the NEUROMARK System in Subjects With Chronic Rhinitis (PARAGON)COMPLETEDNCT05937308NEUROMARK Registry StudyACTIVE_NOT_RECRUITING
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