510(k) · Cleared
ClearedVisicoil MR Marker (User Loaded), Visicoil MR Marker (Pre-Loaded)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Radiomed Corporation · IYE Accelerator, Linear, Medical
Cleared on Apr 28, 2017 as substantially equivalent to K070305 (Radiomed Corporation, 2007) after a 310-day review. Its family tree reaches back 6 generations to 1987. 1 later device descends from it.
- Decided
- Apr 28, 2017
- Review
- 310 days
- Class
- Class II
- Product code
- IYE
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 6 generations to K874787 (1987). 11 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 6 generations backK874787 Modified Palladium Seed Model 100Theragenics Corp. · 1987
- 5 generations backK001070 Radiomed SourceRadiomed Corp. · 2000
- 4 generations backK013660 GenetraRadiomed Corporation · 2001
- 3 generations backK022326 Radiomed MarkerRadiomed Corporation · 2003
- 2 generations backK031206 Radiomed Soft Tissue MarkerRadiomed Corp. · 2003
- 1 generation backK070305 Pre-Loaded VisicoilRadiomed Corporation · 2007
- This deviceK161724 Visicoil MR Marker (User Loaded), Visicoil MR Marker (Pre-Loaded)Radiomed Corporation · 2017
- Descendant · cites it directly · 0 of its ownK173251 LumiCoil Platinum Fiducial MarkerBoston Scientific Corporation · 2017
Most influential descendants
Showing 1 of 1 · See all- K173251LumiCoil Platinum Fiducial MarkerBoston Scientific Corporation · 2017 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K874787 | Modified Palladium Seed Model 100 | Theragenics Corp. | 1987 | — |
| −5 | K001070 | Radiomed Source | Radiomed Corp. | 2000 | — |
| −4 | K013660 | Genetra | Radiomed Corporation | 2001 | — |
| −3 | K022326 | Radiomed Marker | Radiomed Corporation | 2003 | — |
| −2 | K031206 | Radiomed Soft Tissue Marker | Radiomed Corp. | 2003 | — |
| −1 | K070305 | Pre-Loaded Visicoil | Radiomed Corporation | 2007 | — |
| 0 (this device) | K161724 | Visicoil MR Marker (User Loaded), Visicoil MR Marker (Pre-Loaded) | Radiomed Corporation | 2017 | — |
| +1 | K173251 | LumiCoil Platinum Fiducial Marker | Boston Scientific Corporation | 2017 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1994 | 2 | 0 |
| 1997 | 1 | 0 |
| 1999 | 1 | 0 |
| 2000 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2017 | 1 | 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.
Planning a device in IYE? 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 IYE device
- #1 K252977 Halcyon, Ethos Radiotherapy System (5.0)score 18.8 · 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? (1)
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 |
|---|---|---|---|
| * | K070305 | Pre-Loaded VisicoilSummary page 4…entification of Predicate or Legally Marketed Device The predicate devices for RadioMed™ Visicoil MR Marker are: 1. Pre-loaded Visicoil Marker (K070305) Other Reference Devices: 2. Visicoil Marker (K031206) 4. Summary Device Description Device I… | 2007 |
| † | K031206 | Radiomed Soft Tissue Marker | 2003 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K173251 | LumiCoil Platinum Fiducial Marker | 2017 | 0 |
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 30 years and passes through 3 companies; a new generation was cleared every 3.8 years on median.
- None of the 11 ancestors has a recall.
- Of its descendants, K173251 (Boston Scientific Corporation, 2017) has gone furthest, with 0 descendants of its own.
- 5 other devices also cite its predicate K070305.
How does its category compare?
All IYE devicesIYE Accelerator, Linear, Medical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.
FDA decisions per year · IYE
12in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · IYE
170in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IYE
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IYE
101in 2025
MAUDE reports naming product code IYE, 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 | 23 | 44 | 78 | 155 |
| 2008 | 14 | 69 | 49 | 114 |
| 2009 | 20 | 63 | 22 | 174 |
| 2010 | 23 | 74 | 27 | 246 |
| 2011 | 11 | 94 | 73 | 280 |
| 2012 | 28 | 106 | 20 | 128 |
| 2013 | 18 | 88 | 11 | 96 |
| 2014 | 20 | 100 | 14 | 124 |
| 2015 | 20 | 108 | 8 | 100 |
| 2016 | 21 | 97 | 7 | 97 |
| 2017 | 23 | 94 | 7 | 125 |
| 2018 | 21 | 58 | 7 | 85 |
| 2019 | 19 | 83 | 2 | 91 |
| 2020 | 20 | 67 | 4 | 74 |
| 2021 | 19 | 86 | 5 | 68 |
| 2022 | 12 | 172 | 3 | 66 |
| 2023 | 18 | 129 | 7 | 128 |
| 2024 | 9 | 239 | 1 | 81 |
| 2025 | 12 | 170 | 1 | 101 |
| 2026 | 14 | 120 | 4 | — |
What is it indicated for?
The Visicoil MR Marker and the Pre-Loaded Visicoil MR Marker are indicated for use to radiographically mark soft tissue for future therapeutic procedures.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K161724 · printed Nov 6, 2026
Cite this page
510(k) Report. “K161724: Visicoil MR Marker (User Loaded), Visicoil MR Marker (Pre-Loaded).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K161724
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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