Neurent Medical , Ltd.

Neurent Medical , Ltd. holds 2 FDA 510(k) medical device clearances, first cleared 2025, most recent 2026.

Top product codes for Neurent Medical , Ltd.

GEI — General, Plastic Surgery2 devices

Recent clearances by Neurent Medical , Ltd.

K261833 — NEUROMARK System (NMK00301)Code GEI·2026-06-16
K250048 — NEUROMARK System (NMK00301)Code GEI·2025-05-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.