Neuroone Medical Technologies Corp.

Neuroone Medical Technologies Corp. holds 4 FDA 510(k) medical device clearances, first cleared 2021, most recent 2025.

Top product codes for Neuroone Medical Technologies Corp.

Recent clearances by Neuroone Medical Technologies Corp.

K251243 — OneRF Trigeminal Nerve Radiofrequency ProbesCode GXI·2025-08-15
K231675 — OneRF Ablation SystemCode GXD·2023-12-06
K222404 — Evo® sEEG SystemCode GZL·2022-10-20
K211367 — Evo sEEG SystemCode GZL·2021-09-01

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