510(k) Report

510(k) · Cleared

Cleared

MagVita TMS Therapy System

K171481510(k) SpecialCleared Jun 16, 201728-day reviewClass II21 CFR 882.5805

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 · OBP Transcranial Magnetic Stimulator

Cleared on Jun 16, 2017 as substantially equivalent to K160703 (Neuronetics, Inc., 2016) and 1 other predicate after a 28-day review. Its family tree reaches back 5 generations to 2008. 48 later devices descend from it.

Decided
Jun 16, 2017
Review
28 days
Class
Class II
Product code
OBP
Recalls
None
Predicates
2

Its longest line of descent runs back 5 generations to DEN070003 (2008). 6 ancestors in all. 48 later devices descend from it, 7 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2016: 1 other ancestor2025: 12 descendants cleared2020: 1 descendant cleared2018: 2 descendants cleared2023: 10 descendants cleared2017: 1 descendant cleared2024: 5 descendants cleared2022: 3 descendants cleared2019: 3 descendants cleared2021: 2 descendants cleared2026: 9 descendants clearedReference device: K091940 · Magpro, Models R30 with Magoption, X100, X100 with Magoption · Tonica Elektronik A/S · 2010×2: 2 generations cleared close together, DEN070003 (2008), K083538 (2008) K130233 · Neurostar TMS Therapy System · Neuronetics · 2013K133408 · Neurostar TMS Therapy System · Neuronetics · 2014K150641 · MagVita TMS Therapy System · Tonica Elektronik A/S · 201520052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor 1 generation forward: 7 descendants2 generations forward: 16 descendants3 generations forward: 10 descendants4 generations forward: 9 descendants5 generations forward: 4 descendants6 generations forward: 2 descendants K150641 · MagVita TMS Therapy System · Tonica Elektronik A/S · 2015K133408 · Neurostar TMS Therapy System · Neuronetics · 2014K130233 · Neurostar TMS Therapy System · Neuronetics · 2013K083538 · Neurostar TMS Therapy System, Model 1.1 · Neuronetics · 2008 · recalledDEN070003 · Neurostar TMS System · Neuronetics · 2008−50+5
  1. Root · 5 generations backDEN070003 Neurostar TMS SystemNeuronetics · 2008
  2. 4 generations backK083538 Neurostar TMS Therapy System, Model 1.1Neuronetics · 2008 · Recalled
  3. 3 generations backK130233 Neurostar TMS Therapy SystemNeuronetics · 2013
  4. 2 generations backK133408 Neurostar TMS Therapy SystemNeuronetics · 2014
  5. 1 generation backK150641 MagVita TMS Therapy SystemTonica Elektronik A/S · 2015
  6. This deviceK171481 MagVita TMS Therapy SystemTonica Elektronik A/S · 2017
  7. Descendant · cites it directly · 39 of its ownK173620 Mag Vita TMS Therapy System w/Theta Burst StimulationTonica Elektronik A/S · 2018
  8. Descendant · cites it directly · 24 of its ownK193006 MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS…Tonica Elektronik A/S · 2020
  9. Descendant · 2 generations on · 19 of its ownK212289 NeuroStar Advanced Therapy for adjunctive treatment of OCD…Neuronetics, Inc. · 2022
  10. Descendant · cites it directly · 17 of its ownK173441 Neurosoft TMS (also CloudTMS)Teleemg, LLC · 2017
  11. Descendant · 3 generations on · 13 of its ownK230029 NeuroStar Advanced Therapy System (Version 3.7)Neuronetics · 2023

Showing 5 of 48 descendants. See all descendants

Descendants cleared per year

2017: 12018: 22019: 32020: 12021: 22022: 32023: 102024: 52025: 122026: 9
2017high 12 (2025) · low 1 (2017)2026

Most influential descendants

Showing 5 of 48 · See all
  • K173620Mag Vita TMS Therapy System w/Theta Burst StimulationTonica Elektronik A/S · 2018 · cites it directly39descendants
  • K193006MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS Therapy systemTonica Elektronik A/S · 2020 · cites it directly24descendants
  • K212289NeuroStar Advanced Therapy for adjunctive treatment of OCD, NeuroStar Advanced Therapy…Neuronetics, Inc. · 2022 · 2 generations on19descendants
  • K173441Neurosoft TMS (also CloudTMS)Teleemg, LLC · 2017 · cites it directly17descendants
  • K230029NeuroStar Advanced Therapy System (Version 3.7)Neuronetics · 2023 · 3 generations on13descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5DEN070003Neurostar TMS SystemNeuronetics2008—
−4K083538Neurostar TMS Therapy System, Model 1.1Neuronetics20081
−3K130233Neurostar TMS Therapy SystemNeuronetics2013—
−2K133408Neurostar TMS Therapy SystemNeuronetics2014—
−1K150641MagVita TMS Therapy SystemTonica Elektronik A/S2015—
0 (this device)K171481MagVita TMS Therapy SystemTonica Elektronik A/S2017—
+1K173620Mag Vita TMS Therapy System w/Theta Burst StimulationTonica Elektronik A/S2018—
+1K193006MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS Therapy systemTonica Elektronik A/S2020—
+2K212289NeuroStar Advanced Therapy for adjunctive treatment of OCD, NeuroStar Advanced…Neuronetics, Inc.2022—
+1K173441Neurosoft TMS (also CloudTMS)Teleemg, LLC2017—
+3K230029NeuroStar Advanced Therapy System (Version 3.7)Neuronetics2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
201820
201930
202010
202120
202230
2023100
202450
2025120
202690
FIG. 1 — Lineage of K171481, 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 OBP? 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 OBP device

  1. #1 K251119 MagVenture TMS Therapy Systemscore 21.8 · 11 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? (2)

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
*K160703NeuroStar TMS Therapy System
Summary page 4
…[21 CFR 882.5805, Product Code OBP] Classification: Class II Medical Device Predicate Devices: Neurostar TMS Therapy System, K160703 MagVita TMS Therapy System, K150641 Special Controls: The 510k submission addressed the specia…
Neuronetics, Inc.2016—
*K150641MagVita TMS Therapy System
Summary page 4
…Classification: Class II Medical Device Predicate Devices: Neurostar TMS Therapy System, K160703 MagVita TMS Therapy System, K150641 Special Controls: The 510k submission addressed the special controls required by regulation an…
Tonica Elektronik A/S2015—
†K091940Magpro, Models R30 with Magoption, X100, X100 with MagoptionTonica Elektronik A/S2010—

Also cleared against K160703: 7 other devices →

What descends from it? (48)

See all 48

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

NumberDeviceApplicantDecidedDescendants
K173620Mag Vita TMS Therapy System w/Theta Burst StimulationTonica Elektronik A/S201839
K193006MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS Therapy systemTonica Elektronik A/S202024
K173441Neurosoft TMS (also CloudTMS)Teleemg, LLC201717
K251125MagVenture TMS Therapy SystemTonica Elektronik A/S20251
K243460Ultimate rTMSBrain Ultimate, Inc.20251
K230735Ultimate rTMS; Yingchi rTMSBrain Ultimate, Inc.20231
K232688NQ TMS for MDD (NQv1-MU-01)Neuroqore, Inc.20230

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 9 years and passes through 2 companies; a new generation was cleared every 1.3 years on median.
  • 1 of the 6 ancestors has a recall of any class.
  • Of its descendants, K173620 (Tonica Elektronik A/S, 2018) has gone furthest, with 39 descendants of its own.
  • 7 other devices also cite its predicate K160703.

How does its category compare?

All OBP devices

OBP Transcranial Magnetic Stimulator: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · OBP

12in 2025

2008: 22013: 22014: 12015: 22016: 32017: 82018: 42019: 32020: 12021: 52022: 62023: 72024: 52025: 122026 (partial year): 8
2007high 12 (2025) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OBP

125in 2025

2016: 101 days median2017: 73 days median2018: 144 days median2019: 156 days median2021: 132 days median2022: 168 days median2023: 119 days median2024: 266 days median2025: 125 days median2026 (partial year): 176 days median
2007high 266 (2024) · low 73 (2017)2026

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

Recalls per year · OBP

1in 2018

2009: 12018: 12026 (partial year): 1
2007high 1 (2009) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · OBP

81in 2025

2009: 32011: 52012: 32013: 12015: 32016: 62017: 32018: 62019: 122020: 122021: 152022: 592023: 432024: 502025: 81
2007high 81 (2025) · low 0 (2007)2025

MAUDE reports naming product code OBP, 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
20082—00
20090—13
20100—00
20110—05
20120—03
20132—01
20141—00
20152—03
2016310106
201787303
2018414416
20193156012
20201—012
20215132015
20226168059
20237119043
20245266050
202512125081
202681761—

What is it indicated for?

The MagVita TMS Therapy System is indicated for the treatment of Major Depressive Disorder in adult patients who have failed to recieve satisfactory improvement from prior antidepressant medication in the current episode

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K171481: MagVita 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/K171481

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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