510(k) Report

510(k) · Cleared

Cleared

MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS Therapy system

K193006510(k) TraditionalCleared Aug 9, 2020286-day reviewClass II21 CFR 882.5802

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Tonica Elektronik A/S · QCI Transcranial Magnetic Stimulation System For Obsessive-Compulsive Disorder

Cleared on Aug 9, 2020 as substantially equivalent to DEN170078 (Brainways, Ltd., 2018) and 6 other predicates after a 286-day review. Its family tree reaches back 8 generations to 2008. 24 later devices descend from it.

Decided
Aug 9, 2020
Review
286 days
Class
Class II
Product code
QCI
Recalls
None
Predicates
7

Its longest line of descent runs back 8 generations to DEN070003 (2008). 15 ancestors in all. 24 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2019: 1 other ancestor2018: 1 other ancestor2017: 3 other ancestors2015: 1 other ancestor2016: 1 other ancestor2024: 3 descendants cleared2023: 7 descendants cleared2022: 1 descendant cleared2025: 7 descendants cleared2026: 6 descendants cleared×2: 2 generations cleared close together, DEN070003 (2008), K083538 (2008) K130233 · Neurostar TMS Therapy System · Neuronetics · 2013K133408 · Neurostar TMS Therapy System · Neuronetics · 2014K143531 · Rapid Therapy System · Magstim Company Limited · 2015 · recalledK160309 · Neurosoft TMS · Teleemg, LLC · 2016K171967 · MagVita TMS Therapy System · Tonica Elektronik A/S · 2017K173620 · Mag Vita TMS Therapy System w/Theta Burst Stimulation · Tonica Elektronik A/S · 201820052010201520202025
  1. Root · 8 generations backDEN070003 Neurostar TMS SystemNeuronetics · 2008
  2. 7 generations backK083538 Neurostar TMS Therapy System, Model 1.1Neuronetics · 2008 · Recalled
  3. 6 generations backK130233 Neurostar TMS Therapy SystemNeuronetics · 2013
  4. 5 generations backK133408 Neurostar TMS Therapy SystemNeuronetics · 2014
  5. 4 generations backK143531 Rapid Therapy SystemMagstim Company Limited · 2015 · Recalled
  6. 3 generations backK160309 Neurosoft TMSTeleemg, LLC · 2016
  7. 2 generations backK171967 MagVita TMS Therapy SystemTonica Elektronik A/S · 2017
  8. 1 generation backK173620 Mag Vita TMS Therapy System w/Theta Burst StimulationTonica Elektronik A/S · 2018
  9. This deviceK193006 MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS…Tonica Elektronik A/S · 2020
  10. Descendant · cites it directly · 19 of its ownK212289 NeuroStar Advanced Therapy for adjunctive treatment of OCD…Neuronetics, Inc. · 2022
  11. Descendant · 2 generations on · 13 of its ownK230029 NeuroStar Advanced Therapy System (Version 3.7)Neuronetics · 2023
  12. Descendant · 3 generations on · 7 of its ownK231926 NeuroStar Advanced Therapy System (All previously cleared models)Neuronetics, Inc. · 2024 · Recalled
  13. Descendant · 2 generations on · 4 of its ownK222171 Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon…Magstim Company, Ltd. · 2023
  14. Descendant · 3 generations on · 3 of its ownK251119 MagVenture TMS Therapy SystemTonica Elektronik A/S · 2025

Showing 5 of 24 descendants. See all descendants

Descendants cleared per year

2022: 12023: 72024: 32025: 72026: 6
2022high 7 (2023) · low 1 (2022)2026

Most influential descendants

Showing 5 of 24 · See all
  • K212289NeuroStar Advanced Therapy for adjunctive treatment of OCD, NeuroStar Advanced Therapy…Neuronetics, Inc. · 2022 · cites it directly19descendants
  • K230029NeuroStar Advanced Therapy System (Version 3.7)Neuronetics · 2023 · 2 generations on13descendants
  • K231926NeuroStar Advanced Therapy System (All previously cleared models)Neuronetics, Inc. · 2024 · 3 generations on7descendants
  • K222171Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon…Magstim Company, Ltd. · 2023 · 2 generations on4descendants
  • K251119MagVenture TMS Therapy SystemTonica Elektronik A/S · 2025 · 3 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8DEN070003Neurostar TMS SystemNeuronetics2008—
−7K083538Neurostar TMS Therapy System, Model 1.1Neuronetics20081
−6K130233Neurostar TMS Therapy SystemNeuronetics2013—
−5K133408Neurostar TMS Therapy SystemNeuronetics2014—
−4K143531Rapid Therapy SystemMagstim Company Limited20153
−3K160309Neurosoft TMSTeleemg, LLC2016—
−2K171967MagVita TMS Therapy SystemTonica Elektronik A/S2017—
−1K173620Mag Vita TMS Therapy System w/Theta Burst StimulationTonica Elektronik A/S2018—
0 (this device)K193006MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS Therapy systemTonica Elektronik A/S2020—
+1K212289NeuroStar Advanced Therapy for adjunctive treatment of OCD, NeuroStar Advanced…Neuronetics, Inc.2022—
+2K230029NeuroStar Advanced Therapy System (Version 3.7)Neuronetics2023—
+3K231926NeuroStar Advanced Therapy System (All previously cleared models)Neuronetics, Inc.20241
+2K222171Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0…Magstim Company, Ltd.2023—
+3K251119MagVenture TMS Therapy SystemTonica Elektronik A/S2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201510
201610
201730
201810
201910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
202370
202430
202570
202660
FIG. 1 — Lineage of K193006, 2008–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in QCI? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new QCI device

  1. #1 K212289 NeuroStar Advanced Therapy for adjunctive…score 17.7 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (7)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*DEN170078Brainsway Deep Transcranial Magnetic Stimulation (DTMS) System
Summary page 4
…Primary Predicate Brainsway Deep Transcranial Magnetic Stimulation (DTMS) system, HAC – H7 coil (DEN170078, K183303) 21 CFR 882.5802, Transcranial Magnetic Stimulation System f…
Brainways, Ltd.2018—
*K183303Brainsway Deep TMS System
Summary page 4
…Primary Predicate Brainsway Deep Transcranial Magnetic Stimulation (DTMS) system, HAC – H7 coil (DEN170078, K183303) 21 CFR 882.5802, Transcranial Magnetic Stimulation System for Neurol…
Brainsway, Ltd.2019—
*K150641MagVita TMS Therapy System
Summary page 5
…of OCD Class II Predicates MagVenture TMS Therapy system (K150641, K171481, K171967, K172667, K173620) 21 CFR 882.5805, Repetitive Tran…
Tonica Elektronik A/S2015—
*K171481MagVita TMS Therapy System
Summary page 5
…of OCD Class II Predicates MagVenture TMS Therapy system (K150641, K171481, K171967, K172667, K173620) 21 CFR 882.5805, Repetitive Transcranial…
Tonica Elektronik A/S2017—
*K171967MagVita TMS Therapy System
Summary page 5
…Class II Predicates MagVenture TMS Therapy system (K150641, K171481, K171967, K172667, K173620) 21 CFR 882.5805, Repetitive Transcranial Magnetic…
Tonica Elektronik A/S2017—
*K172667MagVita TMS Therapy w/MagPro R20
Summary page 5
…Class II Predicates MagVenture TMS Therapy system (K150641, K171481, K171967, K172667, K173620) 21 CFR 882.5805, Repetitive Transcranial Magnetic Stimulati…
Tonica Elektronik A/S2017—
*K173620Mag Vita TMS Therapy System w/Theta Burst Stimulation
Summary page 5
…Predicates MagVenture TMS Therapy system (K150641, K171481, K171967, K172667, K173620) 21 CFR 882.5805, Repetitive Transcranial Magnetic Stimulation…
Tonica Elektronik A/S2018—

Also cleared against DEN170078: 2 other devices →

What descends from it? (24)

See all 24

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K212289NeuroStar Advanced Therapy for adjunctive treatment of OCD, NeuroStar Advanced Therapy…Neuronetics, Inc.202219
K230657BTL-99-OCBTL Industries, Inc.20241
K221129CloudTMS for OCDTeleemg, LLC20231
K243459Ultimate rTMS for OCD (M-series)Brain Ultimate, Inc.20250

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 12 years and passes through 4 companies; a new generation was cleared every 1.1 years on median.
  • 2 of the 15 ancestors have a recall of any class.
  • Of its descendants, K212289 (Neuronetics, Inc., 2022) has gone furthest, with 19 descendants of its own.
  • 2 other devices also cite its predicate DEN170078.

How does its category compare?

All QCI devices

QCI Transcranial Magnetic Stimulation System For Obsessive-Compulsive Disorder: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · QCI

1in 2025

2018: 12019: 12020: 12022: 12023: 32024: 12025: 1
2007high 3 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QCI

30in 2023

2023: 30 days median
2007high 30 (2023)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · QCI

No recall names QCI since 2007.

Adverse event reports per year · QCI

2in 2024

2019: 12021: 52022: 22024: 2
2007high 5 (2021) · low 0 (2007)2025

MAUDE reports naming product code QCI, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20181—00
20191—01
20201—00
20210—05
20221—02
202333000
20241—02
20251—00
20260—0—

What is it indicated for?

The MagVenture TMS Therapy System is intended to be used as an adjunct for the treatment of adult patients suffering from Obsessive-Compulsive Disorder (OCD).

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K193006: MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS Therapy system.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K193006

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026