510(k) Report

510(k) · Cleared

Cleared

Sonixgps Needle Sensor

K111818510(k) TraditionalCleared Jun 13, 2012351-day reviewClass II21 CFR 892.1560

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

Ultrasonix Medical Corporation · IYO System, Imaging, Pulsed Echo, Ultrasonic

Cleared on Jun 13, 2012 as substantially equivalent to K092619 (Civco, 2009) after a 351-day review. Its family tree reaches back 7 generations to 1994. 6 of the 82 devices in its family, counting itself, have a Class I recall. 15 later devices descend from it.

Decided
Jun 13, 2012
Review
351 days
Class
Class II
Product code
IYO
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K911783 (1994). 66 ancestors in all, the oldest K844472 (1985). 15 later devices descend from it, 2 citing it directly. 6 of the 82 devices in this family, counting this one, have a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2007: 2 other ancestors2004: 2 other ancestors, 1 with a Class I recall12003: 6 other ancestors2000: 5 other ancestors1998: 7 other ancestors, 1 with a Class I recall11997: 3 other ancestors1988: 1 other ancestor2005: 4 other ancestors2002: 7 other ancestors2001: 8 other ancestors1999: 5 other ancestors1996: 3 other ancestors, 1 with a Class I recall11995: 1 other ancestor1993: 1 other ancestor1985: 2 other ancestors1986: 1 other ancestor2014: 2 descendants cleared2020: 3 descendants cleared2019: 2 descendants cleared2022: 3 descendants cleared2021: 2 descendants cleared2023: 1 descendant cleared2026: 2 descendants clearedK911783 · Allegro Viewing Wand · I.S.G. Technologies, Inc. · 1994×2: 2 generations cleared close together, K981998 (1998), K983529 (1998) K994270 · Instatrak 3000 System with Fluorotrak Module, Model IT3000 · Visualization Technology, Inc. · 2000 · Class I recallK053610 · Abaris · Traxtal Technologies, Inc. · 2006 · recalledK080624 · Navstationirad Emt, Version 1.1 · Cas Innovations AG · 2008K092619 · Etrax Needle System, Etrax Variable Angle Needle Guidance System, Virtutrax Universal Tracker · Civco · 2009 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 8 other ancestors, 1 with a Class I recall13 generations back: 38 other ancestors, 2 with a Class I recall24 generations back: 10 other ancestors5 generations back: 2 other ancestors6 generations back: 1 other ancestor 1 generation forward: 2 descendants2 generations forward: 2 descendants3 generations forward: 2 descendants4 generations forward: 1 descendant5 generations forward: 3 descendants6 generations forward: 2 descendants7 generations forward: 1 descendant8 generations forward: 1 descendant9 generations forward: 1 descendant K092619 · Etrax Needle System, Etrax Variable Angle Needle Guidance System, Virtutrax Universal Tracker · Civco · 2009 · recalledK080624 · Navstationirad Emt, Version 1.1 · Cas Innovations AG · 2008K053610 · Abaris · Traxtal Technologies, Inc. · 2006 · recalledK994270 · Instatrak 3000 System with Fluorotrak Module, Model IT3000 · Visualization Technology, Inc. · 2000 · Class I recallK983529 · Instatrak 3000 · Visualization Technology, Inc. · 1998 · Class I recallK981998 · Pediatric Instatrak System · Visualization Technology, Inc. · 1998 · Class I recallK911783 · Allegro Viewing Wand · I.S.G. Technologies, Inc. · 1994−50+5
  1. Root · 7 generations backK911783 Allegro Viewing WandI.S.G. Technologies, Inc. · 1994
  2. 6 generations backK981998 Pediatric Instatrak SystemVisualization Technology, Inc. · 1998 · Recalled (Class I)
  3. 5 generations backK983529 Instatrak 3000Visualization Technology, Inc. · 1998 · Recalled (Class I)
  4. 4 generations backK994270 Instatrak 3000 System with Fluorotrak Module, Model IT3000Visualization Technology, Inc. · 2000 · Recalled (Class I)
  5. 3 generations backK053610 AbarisTraxtal Technologies, Inc. · 2006 · Recalled
  6. 2 generations backK080624 Navstationirad Emt, Version 1.1Cas Innovations AG · 2008
  7. 1 generation backK092619 Etrax Needle System, Etrax Variable Angle Needle Guidance System…Civco · 2009 · Recalled
  8. This deviceK111818 Sonixgps Needle SensorUltrasonix Medical Corporation · 2012
  9. Descendant · cites it directly · 13 of its ownK140254 EZONO 4000Ezono AG · 2014
  10. Descendant · 2 generations on · 10 of its ownK182894 HM70A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2019
  11. Descendant · 3 generations on · 9 of its ownK191055 HS40 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2019
  12. Descendant · 4 generations on · 8 of its ownK200339 HS40 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2020
  13. Descendant · 5 generations on · 4 of its ownK210713 HM70 EVO Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2021

Showing 5 of 15 descendants. See all descendants

Descendants cleared per year

2014: 22019: 22020: 32021: 22022: 32023: 12026: 2
2014high 3 (2020) · low 0 (2015)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 15 · See all
  • K140254EZONO 4000Ezono AG · 2014 · cites it directly13descendants
  • K182894HM70A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2019 · 2 generations on10descendants
  • K191055HS40 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2019 · 3 generations on9descendants
  • K200339HS40 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2020 · 4 generations on8descendants
  • K210713HM70 EVO Diagnostic Ultrasound SystemSamsung Medison Co., Ltd. · 2021 · 5 generations on4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K911783Allegro Viewing WandI.S.G. Technologies, Inc.1994—
−6K981998Pediatric Instatrak SystemVisualization Technology, Inc.1998Class I
−5K983529Instatrak 3000Visualization Technology, Inc.1998Class I
−4K994270Instatrak 3000 System with Fluorotrak Module, Model IT3000Visualization Technology, Inc.2000Class I
−3K053610AbarisTraxtal Technologies, Inc.20063
−2K080624Navstationirad Emt, Version 1.1Cas Innovations AG2008—
−1K092619Etrax Needle System, Etrax Variable Angle Needle Guidance System, Virtutrax…Civco200917
0 (this device)K111818Sonixgps Needle SensorUltrasonix Medical Corporation2012—
+1K140254EZONO 4000Ezono AG2014—
+2K182894HM70A Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2019—
+3K191055HS40 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2019—
+4K200339HS40 Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2020—
+5K210713HM70 EVO Diagnostic Ultrasound SystemSamsung Medison Co., Ltd.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198520
198610
198810
199310
199510
199631
199730
199871
199950
200050
200180
200270
200360
200421
200540
200720
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201420
201920
202030
202120
202230
202310
202620
FIG. 1 — Lineage of K111818, 1994–2026Source: 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.

6 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 IYO device

  1. #1 K243937 Accuro 3Sscore 20.5 · 18 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K092619Etrax Needle System, Etrax Variable Angle Needle Guidance System, Virtutrax Universal…
Summary page 1
…Classification Regulation: 21 CFR 892.1560 Classification Panel: Radiology Il. Predicate Device The SonixG PSm Needle Sensor is substantially equivalent to K092619 - Electromagnetic Tracking System. Page 5-1 ==…
Civco200917

Also cleared against K092619: 5 other devices →

What descends from it? (15)

See all 15

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

NumberDeviceApplicantDecidedDescendants
K140254EZONO 4000Ezono AG201413
K133901Pari-Path Surgical Navigation SystemParitic, Inc.20140

Has anything in its family been recalled? (6 Class I)

No FDA recall names this device.

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.

  • K040050Instatrak System with Multiple Dataset Navigation, Model IT3500Ge Medical Systems Navigation and Visualization IN · 2004 · 2 generations back · ◆ in the 2004 ancestors bar of FIG. 11 Class I recall
  • K994270Instatrak 3000 System with Fluorotrak Module, Model IT3000Visualization Technology, Inc. · 2000 · 3 generations back · ◆ on the line of descent in FIG. 12 Class I recalls
  • K983529Instatrak 3000Visualization Technology, Inc. · 1998 · 3 generations back · ◆ on the line of descent in FIG. 11 Class I recall
  • K982994Skull Base Instatrak SystemVisualization Technology, Inc. · 1998 · 3 generations back · ◆ in the 1998 ancestors bar of FIG. 11 Class I recall
  • K981998Pediatric Instatrak SystemVisualization Technology, Inc. · 1998 · 3 generations back · ◆ on the line of descent in FIG. 11 Class I recall
  • K960330InstatrakVisualization Technology, Inc. · 1996 · 3 generations back · ◆ in the 1996 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 18 years and passes through 6 companies; a new generation was cleared every 2.0 years on median.
  • 22 of the 66 ancestors have a recall of any class; 6 have a Class I recall.
  • Of its descendants, K140254 (Ezono AG, 2014) has gone furthest, with 13 descendants of its own.
  • 5 other devices also cite its predicate K092619.

How does its category compare?

All IYO devices

IYO System, Imaging, Pulsed Echo, Ultrasonic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · IYO

7in 2025

2007: 202008: 142009: 132010: 152011: 112012: 152013: 172014: 142015: 192016: 102017: 192018: 142019: 132020: 112021: 152022: 52023: 112024: 102025: 72026 (partial year): 10
2007high 20 (2007) · low 5 (2022)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IYO

171in 2025

2007: 17 days median2008: 36 days median2009: 79 days median2010: 113 days median2011: 69 days median2012: 68 days median2013: 50 days median2014: 63 days median2015: 46 days median2016: 36 days median2017: 72 days median2018: 56 days median2019: 59 days median2020: 57 days median2021: 64 days median2022: 190 days median2023: 177 days median2024: 220 days median2025: 171 days median2026 (partial year): 139 days median
2007high 220 (2024) · low 17 (2007)2026

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

Recalls per year · IYO

1in 2022

2007: 42008: 52009: 92010: 82012: 22013: 32014: 22015: 12018: 12019: 12021: 112022: 12026 (partial year): 1
2007high 11 (2021) · low 0 (2011)2026

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

Adverse event reports per year · IYO

485in 2025

2007: 392008: 202009: 272010: 202011: 582012: 782013: 4362014: 3042015: 2682016: 2542017: 2382018: 3682019: 5372020: 4982021: 6172022: 5112023: 5272024: 6402025: 485
2007high 640 (2024) · low 20 (2008)2025

MAUDE reports naming product code IYO, 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
20072017439
20081436520
20091379927
201015113820
20111169058
20121568278
201317503436
201414632304
201519461268
201610360254
201719720238
201814561368
201913591537
202011570498
2021156411617
202251901511
2023111770527
2024102200640
202571710485
2026101391—

What is it indicated for?

The device is intended to provide physicians with tools for electromagnetic tracking of instruments with respect to image data. The device is available in two models 0.55mm and 0.9mm in diameter.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K111818: Sonixgps Needle Sensor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111818

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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