510(k) · Cleared
Recalled · 2011Magnetom Trio System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Siemens Medical Systems, Inc. · LNH System, Nuclear Magnetic Resonance Imaging
Cleared on Dec 28, 2001 after a 59-day review. The FDA summary names its predicate without a number. 22 of the 437 devices in its family, counting itself, have a Class I recall. 436 later devices descend from it. It has been recalled 4 times.
- Decided
- Dec 28, 2001
- Review
- 59 days
- Class
- Class II
- Product code
- LNH
- Recalls
- 4
- Predicates
- 0
436 later devices descend from it, 3 citing it directly. 22 of the 437 devices in this family, counting this one, have a Class I recall.
- This deviceK013586 Magnetom Trio SystemSiemens Medical Systems, Inc. · 2001
- Descendant · cites it directly · 428 of its ownK050200 Magnetom Trio a Tim SystemSiemens Medical Solutions USA, Inc. · 2005 · Recalled
- Descendant · 2 generations on · 312 of its ownK052164 Magnetom Systems with Software Syngo MR 2006ASiemens Medical Solutions USA, Inc. · 2005
- Descendant · 2 generations on · 308 of its ownK062454 Magnetom Systems - I-Class and T-Class ReleasesSiemens Medi Cal Solutions, Inc. · 2006
- Descendant · 2 generations on · 300 of its ownK072237 Magnetom VerioSiemens Medical Solutions USA, Inc. · 2007 · Recalled (Class I)
- Descendant · 3 generations on · 229 of its ownK082427 Syngo MR B17Siemens Medical Solutions USA, Inc. · 2008
Showing 5 of 436 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
Most influential descendants
Showing 5 of 436 · See all- K050200Magnetom Trio a Tim SystemSiemens Medical Solutions USA, Inc. · 2005 · cites it directly428descendants
- K052164Magnetom Systems with Software Syngo MR 2006ASiemens Medical Solutions USA, Inc. · 2005 · 2 generations on312descendants
- K062454Magnetom Systems - I-Class and T-Class ReleasesSiemens Medi Cal Solutions, Inc. · 2006 · 2 generations on308descendants
- K072237Magnetom VerioSiemens Medical Solutions USA, Inc. · 2007 · 2 generations on300descendants
- K082427Syngo MR B17Siemens Medical Solutions USA, Inc. · 2008 · 3 generations on229descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K013586 | Magnetom Trio System | Siemens Medical Systems, Inc. | 2001 | — |
| +1 | K050200 | Magnetom Trio a Tim System | Siemens Medical Solutions USA, Inc. | 2005 | 3 |
| +2 | K052164 | Magnetom Systems with Software Syngo MR 2006A | Siemens Medical Solutions USA, Inc. | 2005 | — |
| +2 | K062454 | Magnetom Systems - I-Class and T-Class Releases | Siemens Medi Cal Solutions, Inc. | 2006 | — |
| +2 | K072237 | Magnetom Verio | Siemens Medical Solutions USA, Inc. | 2007 | Class I |
| +3 | K082427 | Syngo MR B17 | Siemens Medical Solutions USA, Inc. | 2008 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2002 | 1 | 0 |
| 2004 | 1 | 0 |
| 2005 | 3 | 0 |
| 2006 | 5 | 0 |
| 2007 | 4 | 1 |
| 2008 | 8 | 0 |
| 2009 | 5 | 0 |
| 2010 | 6 | 1 |
| 2011 | 14 | 0 |
| 2012 | 13 | 2 |
| 2013 | 23 | 2 |
| 2014 | 16 | 0 |
| 2015 | 18 | 1 |
| 2016 | 15 | 1 |
| 2017 | 23 | 1 |
| 2018 | 26 | 2 |
| 2019 | 29 | 1 |
| 2020 | 39 | 3 |
| 2021 | 18 | 1 |
| 2022 | 37 | 2 |
| 2023 | 42 | 3 |
| 2024 | 31 | 0 |
| 2025 | 32 | 1 |
| 2026 | 27 | 0 |
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.
22 devices in this family have a Class I recall. 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 LNH device
- #1 K213693 MAGNETOM Vida with syngo MR XA50Ascore 23.0 · 18 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (4)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | — | MAGNETOM 3.0 T Allegra Dedicated Head only System Named without a submission number | |
| * | — | GE’s Body Imaging Coil for 3.0T Signa VH /1 system Named without a submission number | |
| * | — | MAGNETOM 1.5 T Sonata System Named without a submission number | |
| * | — | 3.0 T Dedicated Head Only Allegra System Named without a submission number |
What descends from it? (436)
See all 4363 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (22 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Mar 3, 2011 | Not classified | Z-2021-2011 | Other | Firm discovered during product monitoring that on a few systems the gradient cable connections did not meet their specifications after installation. The potential exists for a cable connection to become overheated, leading to the emission… |
| Jul 28, 2004 | Not classified | Z-1403-04 | Other | An input error can be made with Magnetom MRI software. Software allows users to manually change Transmit Reference Voltage in certain windows |
| Jul 28, 2004 | Not classified | Z-1404-04 | Other | An input error can be made with Magnetom MRI software. Software allows users to manually change Transmit Reference Voltage in certain windows |
| Dec 18, 2003 | Not classified | Z-0521-04 | Other | tissue roll can become magnetic |
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K072237Magnetom VerioSiemens Medical Solutions USA, Inc. · 2007 · 2 generations on · ◆ in the 2007 descendants bar of FIG. 11 Class I recall
- K101347Magnetom Aera; Magnetom SkyraSiemens Medical Solutions USA, Inc. · 2010 · 3 generations on · ◆ in the 2010 descendants bar of FIG. 12 Class I recalls
- K130885Magnetom Avanto-Fit, Magnetom Skyra-FitSiemens Medical Solutions USA, Inc. · 2013 · 3 generations on · ◆ in the 2013 descendants bar of FIG. 11 Class I recall
- K121160Magnetom SpectraSiemens Medical Solutions USA, Inc. · 2012 · 3 generations on · ◆ in the 2012 descendants bar of FIG. 11 Class I recall
- K121434Software Syngo MR D13A for the Magnetom Systems Aera/Skyra/Avanto/VerioSiemens Medi Cal Solutions, Inc. · 2012 · 4 generations on · ◆ in the 2012 descendants bar of FIG. 12 Class I recalls
- K181613MAGNETOM Avanto, MAGNETOM Verio with software syngo MR E11DSiemens Medical Solutions USA, Inc. · 2018 · 5 generations on · ◆ in the 2018 descendants bar of FIG. 12 Class I recalls
- K132119Magnetom Prisma, Magnetom Prisma FitSiemens Medical Solutions USA, Inc. · 2013 · 5 generations on · ◆ in the 2013 descendants bar of FIG. 11 Class I recall
- K153343MAGNETOM Aera, MAGNETOM Skyra, MAGNETOM Prisma, MAGNETOM Prisma fitSiemens Medi Cal Solutions, Inc. · 2016 · 6 generations on · ◆ in the 2016 descendants bar of FIG. 11 Class I recall
- K151579MAGNETOM Aera (24-channel), MAGNETOM Avanto fit, MAGNETOM Skyra fit, MAGNETOM Prisma, MAGNETOM Prisma fitSiemens Medical Solutions USA, Inc. · 2015 · 6 generations on · ◆ in the 2015 descendants bar of FIG. 12 Class I recalls
- K200213Biograph mMR with syngo MR E11P-AP01 system softwareSiemens Medical Solutions USA, Inc. · 2020 · 6 generations on · ◆ in the 2020 descendants bar of FIG. 11 Class I recall
- K170396MAGNETOM VidaSiemens Medical Solutions USA, Inc. · 2017 · 7 generations on · ◆ in the 2017 descendants bar of FIG. 11 Class I recall
- K173592MAGNETOM Aera, MAGNETOM Skyra/Skyrafit, MAGNETOM Prisma/Prismafit, MAGNETOM AvantofitSiemens Medical Solutions USA, Inc. · 2018 · 7 generations on · ◆ in the 2018 descendants bar of FIG. 12 Class I recalls
Nearest 12 of 22 shown.
Nearest 5 of 22; all are on the web page.
What does this lineage say?
- Of its descendants, K050200 (Siemens Medical Solutions USA, Inc., 2005) has gone furthest, with 428 descendants of its own.
How does its category compare?
All LNH devicesLNH System, Nuclear Magnetic Resonance Imaging: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · LNH
26in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LNH
122in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LNH
8in 2025
Class I (8 since 2007) Class II/III not classified
Adverse event reports per year · LNH
1,263in 2025
MAUDE reports naming product code LNH, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 12 | 35 | 25 | 114 |
| 2008 | 19 | 53 | 12 | 167 |
| 2009 | 17 | 70 | 7 | 194 |
| 2010 | 12 | 94 | 17 | 165 |
| 2011 | 16 | 81 | 11 | 182 |
| 2012 | 22 | 89 | 5 | 170 |
| 2013 | 19 | 108 | 2 | 107 |
| 2014 | 17 | 108 | 13 | 119 |
| 2015 | 19 | 140 | 12 (2) | 113 |
| 2016 | 20 | 108 | 1 | 135 |
| 2017 | 18 | 98 | 0 | 121 |
| 2018 | 29 | 128 | 71 | 158 |
| 2019 | 26 | 62 | 5 | 158 |
| 2020 | 32 | 121 | 4 | 98 |
| 2021 | 27 | 87 | 41 | 84 |
| 2022 | 30 | 74 | 13 | 138 |
| 2023 | 30 | 124 | 10 (1) | 159 |
| 2024 | 26 | 104 | 4 | 281 |
| 2025 | 26 | 122 | 8 (5) | 1,263 |
| 2026 | 24 | 126 | 43 | — |
What is it indicated for?
The MAGNETOM Trio system is a whole body scanner designed to support higher resolution imaging and shorter scan times. The Trio system is indicated for use as a diagnostic imaging device to produce transverse, sagittal, coronal and oblique images of the internal structures of the head and whole body. The images produced by the Trio system reflect the spatial distribution of protons (hydrogen nuclei) exhibiting magnetic resonance. The NMR properties that determine the image appearance are proton density, spin-lattice relaxation time (T1), spin-spin echo time (T2) and flow. When interpreted by a trained physician, these images provide information that can be useful in determining diagnosis.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K013586 · printed Nov 4, 2026
Cite this page
510(k) Report. “K013586: Magnetom Trio System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K013586
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026