510(k) · Cleared
ClearedOstial Pro Stent Positioning System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Ostial Solutions, LLC · DQX Wire, Guide, Catheter
Cleared on May 24, 2007 as substantially equivalent to K994358 (Cordis Corp., 2000) and 3 other predicates after a 297-day review. Its family tree reaches back 4 generations to 1997. 5 of the 52 devices in its family, counting itself, have a Class I recall. 35 later devices descend from it.
- Decided
- May 24, 2007
- Review
- 297 days
- Class
- Class II
- Product code
- DQX
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 4 generations to K970376 (1997). 16 ancestors in all, the oldest K893626 (1989). 35 later devices descend from it, 4 citing it directly. 5 of the 52 devices in this family, counting this one, have a Class I recall.
- Root · 4 generations backK970376 Ptca GuidewireLake Region Mfg., Inc. · 1997
- 3 generations backK011968 Streerable Ptca GuidewireLake Region Mfg., Inc. · 2001 · Recalled
- 2 generations backK022813 Steerable GuidewireLake Region Mfg., Inc. · 2003
- 1 generation backK042338 Coronary Peripheral and Renal Steerable GuidewireLake Region Mfg., Inc. · 2004
- This deviceK062192 Ostial Pro Stent Positioning SystemOstial Solutions, LLC · 2007
- Descendant · cites it directly · 30 of its ownK083745 The IC-Pro System, Model Version 3.2Paieon, Inc. · 2009
- Descendant · 2 generations on · 15 of its ownK110256 The IC-Pro SystemPaieon, Inc. · 2011
- Descendant · 2 generations on · 13 of its ownK100292 Caas Qva 3D, Caas Qca 3DPie Medical Imaging BV · 2010
- Descendant · 2 generations on · 11 of its ownK091781 Guided Medical Positioning System (GMPS)Mediguide, Ltd. · 2009
- Descendant · 3 generations on · 10 of its ownK133993 Caas WorkstationPie Medical Imaging · 2014
Showing 5 of 35 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K190106 Intra-Operative Positioning System; Simple Curve…4 generations on · 2019
- K242133 Intra-Operative Positioning System (IOPS®)…5 generations on · 2024
- K241243 Intra-Operative Positioning System (IOPS®)…5 generations on · 2024
- K230309 Intra-Operative Positioning System (IOPS®)…5 generations on · 2023
Most influential descendants
Showing 5 of 35 · See all- K083745The IC-Pro System, Model Version 3.2Paieon, Inc. · 2009 · cites it directly30descendants
- K110256The IC-Pro SystemPaieon, Inc. · 2011 · 2 generations on15descendants
- K100292Caas Qva 3D, Caas Qca 3DPie Medical Imaging BV · 2010 · 2 generations on13descendants
- K091781Guided Medical Positioning System (GMPS)Mediguide, Ltd. · 2009 · 2 generations on11descendants
- K133993Caas WorkstationPie Medical Imaging · 2014 · 3 generations on10descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K970376 | Ptca Guidewire | Lake Region Mfg., Inc. | 1997 | — |
| −3 | K011968 | Streerable Ptca Guidewire | Lake Region Mfg., Inc. | 2001 | 2 |
| −2 | K022813 | Steerable Guidewire | Lake Region Mfg., Inc. | 2003 | — |
| −1 | K042338 | Coronary Peripheral and Renal Steerable Guidewire | Lake Region Mfg., Inc. | 2004 | — |
| 0 (this device) | K062192 | Ostial Pro Stent Positioning System | Ostial Solutions, LLC | 2007 | — |
| +1 | K083745 | The IC-Pro System, Model Version 3.2 | Paieon, Inc. | 2009 | — |
| +2 | K110256 | The IC-Pro System | Paieon, Inc. | 2011 | — |
| +2 | K100292 | Caas Qva 3D, Caas Qca 3D | Pie Medical Imaging BV | 2010 | — |
| +2 | K091781 | Guided Medical Positioning System (GMPS) | Mediguide, Ltd. | 2009 | — |
| +3 | K133993 | Caas Workstation | Pie Medical Imaging | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1989 | 1 | 0 |
| 1991 | 1 | 0 |
| 1995 | 3 | 0 |
| 2000 | 1 | 0 |
| 2001 | 1 | 0 |
| 2002 | 1 | 0 |
| 2003 | 3 | 0 |
| 2006 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 3 | 0 |
| 2010 | 2 | 0 |
| 2011 | 1 | 0 |
| 2012 | 6 | 0 |
| 2013 | 1 | 0 |
| 2014 | 3 | 0 |
| 2015 | 1 | 0 |
| 2016 | 1 | 0 |
| 2018 | 1 | 0 |
| 2019 | 2 | 1 |
| 2021 | 1 | 0 |
| 2023 | 3 | 1 |
| 2024 | 3 | 2 |
| 2025 | 4 | 1 |
| 2026 | 3 | 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.
5 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 DQX device
- #1 K213854 SavvyWirescore 15.7 · 10 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 |
|---|---|---|---|
| * | K994358 | Atw Marker Wire Steerable GuidewireSummary page 1…ct Code: DQX Device Classification: Catheter Guidewire Regulation Number: 870.1330 PREDICATE DEVICES · Cordis® Corporation, ATW TM Marker Wire Steerable Guidewire, K994358 * Lake Region Manufacturing, Inc., Coronary, Peripheral and Renal Steerable Hydrophilic Guidewire, K042338 * EV3… | 2000 |
| * | K042338 | Coronary Peripheral and Renal Steerable GuidewireSummary page 1…rporation, ATW TM Marker Wire Steerable Guidewire, K994358 * Lake Region Manufacturing, Inc., Coronary, Peripheral and Renal Steerable Hydrophilic Guidewire, K042338 * EV3® Inc., Nitrex® Guidewire, K031864 * BioSphere Medical, Inc., Sequitor Steerable Guidewire, K061171… | 2004 |
| * | K031864 | Nitrex Nitinol GuidewireSummary page 1…wire, K994358 * Lake Region Manufacturing, Inc., Coronary, Peripheral and Renal Steerable Hydrophilic Guidewire, K042338 * EV3® Inc., Nitrex® Guidewire, K031864 * BioSphere Medical, Inc., Sequitor Steerable Guidewire, K061171 M… | 2003 |
| * | K061171 | Sequitor Steerable Guidewire, Models SQR18XX and SQR14XXSummary page 1…eral and Renal Steerable Hydrophilic Guidewire, K042338 * EV3® Inc., Nitrex® Guidewire, K031864 * BioSphere Medical, Inc., Sequitor Steerable Guidewire, K061171 M T… | 2006 |
What descends from it? (35)
See all 354 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (5 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.
- K190106Intra-Operative Positioning System; Simple Curve Catheter, Reverse Curve Catheter ; Angled Tip Guidewire…Centerline Biomedical, Inc. · 2019 · 4 generations on · ◆ in the 2019 descendants bar of FIG. 11 Class I recall
- K242133Intra-Operative Positioning System (IOPS®) (Fiducial Tracking Pad); Intra-Operative Positioning System…Centerline Biomedical, Inc. · 2024 · 5 generations on · ◆ in the 2024 descendants bar of FIG. 11 Class I recall
- K241243Intra-Operative Positioning System (IOPS®) Viewpoint (Simple Curve Catheters); Intra-Operative Positioning…Centerline Biomedical, Inc. · 2024 · 5 generations on · ◆ in the 2024 descendants bar of FIG. 11 Class I recall
- K230309Intra-Operative Positioning System (IOPS®) (MC-1); IOPS Simple Curve Catheter (SCC-1) and IOPS Reverse Curve…Centerline Biomedical, Inc. · 2023 · 5 generations on · ◆ in the 2023 descendants bar of FIG. 11 Class I recall
- K243842Intra-Operative Positioning System (IOPS®)Centerline Biomedical, Inc. · 2025 · 5 generations on · ◆ in the 2025 descendants bar of FIG. 11 Class I recall
What does this lineage say?
- The line of descent spans 10 years and passes through 2 companies; a new generation was cleared every 2.7 years on median.
- 1 of the 16 ancestors has a recall of any class.
- Of its descendants, K083745 (Paieon, Inc., 2009) has gone furthest, with 30 descendants of its own.
- 2 other devices also cite its predicate K994358.
How does its category compare?
All DQX devicesDQX Wire, Guide, Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · DQX
10in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DQX
177in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DQX
3in 2024
Class I (8 since 2007) Class II/III not classified
Adverse event reports per year · DQX
2,178in 2025
MAUDE reports naming product code DQX, 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 | 14 | 85 | 12 | 760 |
| 2008 | 19 | 87 | 7 | 715 |
| 2009 | 18 | 87 | 49 | 687 |
| 2010 | 21 | 63 | 34 | 987 |
| 2011 | 18 | 43 | 3 | 1,311 |
| 2012 | 20 | 62 | 5 | 1,337 |
| 2013 | 18 | 119 | 7 (4) | 1,474 |
| 2014 | 18 | 103 | 0 | 1,323 |
| 2015 | 15 | 112 | 1 | 1,323 |
| 2016 | 14 | 179 | 2 (2) | 1,466 |
| 2017 | 19 | 85 | 17 | 1,524 |
| 2018 | 19 | 114 | 9 | 1,737 |
| 2019 | 13 | 173 | 2 | 1,679 |
| 2020 | 14 | 106 | 1 (1) | 1,536 |
| 2021 | 6 | 161 | 0 | 1,713 |
| 2022 | 15 | 212 | 0 | 1,647 |
| 2023 | 10 | 136 | 0 | 2,068 |
| 2024 | 11 | 134 | 3 | 2,210 |
| 2025 | 10 | 177 | 0 | 2,178 |
| 2026 | 12 | 145 | 4 (1) | — |
What is it indicated for?
The Ostial Pro Stent Positioning System is intended for use in aorta-ostial procedures to
introduce and position stents and other interventional devices within the coronary and
peripheral vasculature. In addition, the Ostial Pro Stent Positioning System is intended to
facilitate the alignment of interventional devices and function as an alignment tool.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K062192 · printed Nov 6, 2026
Cite this page
510(k) Report. “K062192: Ostial Pro Stent Positioning System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K062192
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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