Neuronetics, Inc.
Neuronetics, Inc. holds FDA 510(k) medical device clearances, first cleared 2016, most recent 2024, with 1 FDA device recall on record.
Top product codes for Neuronetics, Inc.
FDA recalls by Neuronetics, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Neuronetics, Inc.
- K231926 — NeuroStar Advanced Therapy System (All previously cleared models)
- K222230 — NeuroStar, NeuroStar TMS Therapy System, NeuroStar Advanced Therapy System, NeuroStar Advanced Therapy System for Mental Health
- K220127 — NeuroStar TMS Therapy System, NeuroStar Advanced Therapy System, NeuroStar, NeuroStar Advanced Therapy for Mental Health
- K212289 — NeuroStar Advanced Therapy for adjunctive treatment of OCD, NeuroStar Advanced Therapy System, NeuroStar TMS Therapy System, NeuroStar Advanced Therapy for Mental Health, NeuroStar
- K213543 — NeuroStar TMS Therapy System, NeuroStar Advanced Therapy System, NeuroStar, NeuroStar Advanced Therapy for Mental Health
- K201158 — NeuroStar Advanced Therapy
- K161519 — NeuroStar TMS Therapy System
- K160703 — NeuroStar TMS Therapy System
Data sourced from openFDA. This site is unofficial and independent of the FDA.