510(k) · Cleared
Recalled · Class II · 2015Angiojet Solent Omni Thrombectomy Set
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medrad, Inc. · QEZ Aspiration Thrombectomy Catheter
Cleared on May 24, 2011 as substantially equivalent to K101406 (Medrad Interventional/Possis, 2010) and 1 other predicate after a 27-day review. Its family tree reaches back 11 generations to 1990. 1 of the 49 devices in its family, counting itself, has a Class I recall. 28 later devices descend from it. It has been recalled once.
- Decided
- May 24, 2011
- Review
- 27 days
- Class
- Class II
- Product code
- QEZ
- Recalls
- 1
- Predicates
- 2
Its longest line of descent runs back 11 generations to K901627 (1990). 20 ancestors in all, the oldest K780551 (1978). 28 later devices descend from it, 2 citing it directly. 1 of the 49 devices in this family, counting this one, has a Class I recall.
- Root · 11 generations backK901627 Arterial Embolectomy CatheterApplied Vascular Devices, Inc. · 1990 · Recalled
- 7 generations between
- 3 generations backK090253 Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet…Possis Medical, Inc. · 2009
- 2 generations backK091593 Angio Jet Ultra DVX and Xpeedior Thrombectomy SetsPossis Medical, Inc. · 2009
- 1 generation backK101406 Angiojet Solent Proxi Thrombectomy Set Model 109676-001Medrad Interventional/Possis · 2010
- This deviceK111182 Angiojet Solent Omni Thrombectomy SetMedrad, Inc. · 2011
- Descendant · cites it directly · 26 of its ownK151313 ZelanteDVT Thrombectomy SetBoston Scientific Corporation · 2015
- Descendant · 2 generations on · 21 of its ownK193462 ClotTriever Thrombectomy SystemInari Medical · 2020
- Descendant · 3 generations on · 20 of its ownK210190 ClotTriever Thrombectomy SystemIrani Medical, Inc. · 2021
- Descendant · 4 generations on · 19 of its ownK210689 ClotTriever Thrombectomy SystemInari Medical, Inc. · 2021
- Descendant · 5 generations on · 15 of its ownK212632 ClotTriever Thrombectomy SystemInari Medical, Inc. · 2021
Show all 11 generations
- Root · 11 generations backK901627 Arterial Embolectomy CatheterApplied Vascular Devices, Inc. · 1990 · Recalled
- 10 generations backK960970 Possis Angiojet Rapid Thrombectomy Catheter System, F105…Possis Medical, Inc. · 1996
- 9 generations backK972610 Possis Angiojet Rapid Thombectomy Catheters--F105 Catheter Model…Possis Medical, Inc. · 2000
- 8 generations backK040013 Angiojet Xpeedior 120 Catheter and Angiojet Power Pulse Spray…Possis Medical, Inc. · 2004
- 7 generations backK052256 Angiojet Xpeedior 120 CatheterPossis Medical, Inc. · 2005
- 6 generations backK061951 Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model Xpeedior 120Possis Medical, Inc. · 2006
- 5 generations backK071342 Angiojet Ultra Xpeedior Thrombectomy Set, Model 105040, 105042…Possis Medical, Inc. · 2007
- 4 generations backK072269 Angiojet Ultra DVX Thrombectomy Set, Model: 106552Possis Medical, Inc. · 2007
- 3 generations backK090253 Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet…Possis Medical, Inc. · 2009
- 2 generations backK091593 Angio Jet Ultra DVX and Xpeedior Thrombectomy SetsPossis Medical, Inc. · 2009
- 1 generation backK101406 Angiojet Solent Proxi Thrombectomy Set Model 109676-001Medrad Interventional/Possis · 2010
- This deviceK111182 Angiojet Solent Omni Thrombectomy SetMedrad, Inc. · 2011
Showing 5 of 28 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K223210 ClotTriever XL Catheter6 generations on · 2023
Most influential descendants
Showing 5 of 28 · See all- K151313ZelanteDVT Thrombectomy SetBoston Scientific Corporation · 2015 · cites it directly26descendants
- K193462ClotTriever Thrombectomy SystemInari Medical · 2020 · 2 generations on21descendants
- K210190ClotTriever Thrombectomy SystemIrani Medical, Inc. · 2021 · 3 generations on20descendants
- K210689ClotTriever Thrombectomy SystemInari Medical, Inc. · 2021 · 4 generations on19descendants
- K212632ClotTriever Thrombectomy SystemInari Medical, Inc. · 2021 · 5 generations on15descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −11 | K901627 | Arterial Embolectomy Catheter | Applied Vascular Devices, Inc. | 1990 | 1 |
| −10 | K960970 | Possis Angiojet Rapid Thrombectomy Catheter System, F105 Catheter,Model… | Possis Medical, Inc. | 1996 | — |
| −9 | K972610 | Possis Angiojet Rapid Thombectomy Catheters--F105 Catheter Model 3030C, LF140… | Possis Medical, Inc. | 2000 | — |
| −8 | K040013 | Angiojet Xpeedior 120 Catheter and Angiojet Power Pulse Spray Ancillary Kit | Possis Medical, Inc. | 2004 | — |
| −7 | K052256 | Angiojet Xpeedior 120 Catheter | Possis Medical, Inc. | 2005 | — |
| −6 | K061951 | Angiojet Xpeedior Rheolytic Thrombectomy Catheter, Model Xpeedior 120 | Possis Medical, Inc. | 2006 | — |
| −5 | K071342 | Angiojet Ultra Xpeedior Thrombectomy Set, Model 105040, 105042, 106552… | Possis Medical, Inc. | 2007 | — |
| −4 | K072269 | Angiojet Ultra DVX Thrombectomy Set, Model: 106552 | Possis Medical, Inc. | 2007 | — |
| −3 | K090253 | Angiojet Ultra DVX Thrombectomy Set, Model 106552-001, Angiojet Ultra Xpeedior… | Possis Medical, Inc. | 2009 | — |
| −2 | K091593 | Angio Jet Ultra DVX and Xpeedior Thrombectomy Sets | Possis Medical, Inc. | 2009 | — |
| −1 | K101406 | Angiojet Solent Proxi Thrombectomy Set Model 109676-001 | Medrad Interventional/Possis | 2010 | — |
| 0 (this device) | K111182 | Angiojet Solent Omni Thrombectomy Set | Medrad, Inc. | 2011 | — |
| +1 | K151313 | ZelanteDVT Thrombectomy Set | Boston Scientific Corporation | 2015 | — |
| +2 | K193462 | ClotTriever Thrombectomy System | Inari Medical | 2020 | — |
| +3 | K210190 | ClotTriever Thrombectomy System | Irani Medical, Inc. | 2021 | — |
| +4 | K210689 | ClotTriever Thrombectomy System | Inari Medical, Inc. | 2021 | — |
| +5 | K212632 | ClotTriever Thrombectomy System | Inari Medical, Inc. | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1978 | 1 | 0 |
| 1991 | 1 | 0 |
| 1995 | 1 | 0 |
| 2000 | 1 | 0 |
| 2005 | 1 | 0 |
| 2007 | 2 | 0 |
| 2008 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 1 | 0 |
| 2015 | 1 | 0 |
| 2020 | 2 | 0 |
| 2021 | 3 | 0 |
| 2022 | 2 | 0 |
| 2023 | 9 | 1 |
| 2024 | 3 | 0 |
| 2025 | 4 | 0 |
| 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.
1 device in this family has 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 QEZ device
- #1 K253925 Aventus Thrombectomy Systemscore 17.9 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K101406 | Angiojet Solent Proxi Thrombectomy Set Model 109676-001Summary page 5…[email protected] April 25,2011 AngioJet® Solent™ Omni Thrombectomy Set 870.5150 and 870.1210 DXE and KRA The subject device is equivalent to the following devices: e K101406 AngioJet Ultra Solent Proxi Thrombectomy Set e K091593 AngioJet Ultra Xpeedior Thrombectomy Set AngioJet Solent Omni Thrombectom… | 2010 |
| * | K091593 | Angio Jet Ultra DVX and Xpeedior Thrombectomy SetsSummary page 5…hrombectomy Set 870.5150 and 870.1210 DXE and KRA The subject device is equivalent to the following devices: e K101406 AngioJet Ultra Solent Proxi Thrombectomy Set e K091593 AngioJet Ultra Xpeedior Thrombectomy Set AngioJet Solent Omni Thrombectomy Set is a sterile, single use, disposable set that incl… | 2009 |
What descends from it? (28)
See all 282 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (1 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Jul 31, 2015 | Class II | Z-2378-2015 | Process control | AngioJet products were distributed with an incorrect use-by (expiry) date. The correct date is Nov-2015, but the units are labeled with a use-by date of Dec-2015. |
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.
- K223210ClotTriever XL CatheterInari Medical, Inc. · 2023 · 6 generations on · ◆ in the 2023 descendants bar of FIG. 11 Class I recall
What does this lineage say?
- The line of descent spans 21 years and passes through 4 companies; a new generation was cleared every 1.0 years on median.
- 5 of the 20 ancestors have a recall of any class.
- Of its descendants, K151313 (Boston Scientific Corporation, 2015) has gone furthest, with 26 descendants of its own.
- 1 other device also cites its predicate K101406.
How does its category compare?
All QEZ devicesQEZ Aspiration Thrombectomy Catheter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · QEZ
5in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · QEZ
108in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · QEZ
No recall names QEZ since 2007.
Adverse event reports per year · QEZ
21in 2025
MAUDE reports naming product code QEZ, 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 | 11 | 79 | 0 | 0 |
| 2008 | 6 | 72 | 0 | 0 |
| 2009 | 4 | 83 | 0 | 0 |
| 2010 | 3 | 33 | 0 | 0 |
| 2011 | 7 | 118 | 0 | 0 |
| 2012 | 5 | 90 | 0 | 0 |
| 2013 | 4 | 144 | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 3 | 112 | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 3 | 94 | 0 | 0 |
| 2020 | 3 | 120 | 0 | 0 |
| 2021 | 3 | 53 | 0 | 2 |
| 2022 | 2 | — | 0 | 18 |
| 2023 | 1 | — | 0 | 14 |
| 2024 | 1 | — | 0 | 17 |
| 2025 | 5 | 108 | 0 | 21 |
| 2026 | 6 | 98 | 0 | — |
What is it indicated for?
The AngioJet Solent Omni Thrombectomy Set is intended for use with the AngioJet Ultra Console to break apart and remove thrombus from:
¢ upper and lower extremity peripheral arteries > 3.0mm in diameter,
upper extremity peripheral veins > 3.0mm in diameter,
ileofemoral and lower extremity veins > 3.0mm in diameter,
A-V access conduits > 3.0mm in diameter and
for use with the AngioJet Ultra Power Pulse Kit for the control and selective infusion of
physician specified fluids, including thrombolytic agents, into the peripheral vascular
system.
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/K111182 · printed Nov 6, 2026
Cite this page
510(k) Report. “K111182: Angiojet Solent Omni Thrombectomy Set.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111182
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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