510(k) Report

510(k) · Cleared

Cleared

Indigo Aspiration System - Lightning Aspiration Tubing

K210323510(k) SpecialCleared Feb 26, 202122-day reviewClass II21 CFR 870.5150

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

Penumbra, Inc. · QEW Peripheral Mechanical Thrombectomy With Aspiration

Cleared on Feb 26, 2021 as substantially equivalent to K193244 (Penumbra, Inc., 2020) after a 22-day review. Its family tree reaches back 13 generations to 2001. 11 later devices descend from it.

Decided
Feb 26, 2021
Review
22 days
Class
Class II
Product code
QEW
Recalls
None
Predicates
1

Its longest line of descent runs back 13 generations to K003410 (2001). 15 ancestors in all, the oldest K003086 (2001). 11 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2009: 1 other ancestor2001: 1 other ancestor2023: 1 descendant cleared2022: 1 descendant cleared2024: 4 descendants cleared2025: 2 descendants cleared2026: 3 descendants clearedReference device: K200771 · Indigo Aspiration System Lightning Aspiration Tubing · Penumbra, Inc. · 2020Reference device: K202821 · Indigo Aspiration System - Aspiration Catheter 12 and Separator 12 · Penumbra, Inc. · 2020Reference device: K180939 · Indigo Aspiration System - Modified 110 Aspiration Tubing · Penumbra, Inc. · 2018K003410 · Concentric Retriever, Model 90030 · Concentric Medical, Inc. · 2001 · recalledK030476 · Modified Concentric Retriever, Model 90037 · Concentric Medical, Inc. · 2003 · recalledK033736 · Merci Retriever, Models 90065, 90066 · Concentric Medical, Inc. · 2004K072718 · Penumbra System · Penumbra, Inc. · 2007 · recalledK100769 · Penumbra System Separator Flex (026,032,041,054), Models PSF026, PSF032, PSF041, PSF054 · Penumbra, Inc. · 2010K113163 · Penumbra System Max · Penumbra, Inc. · 2011K121917 · Penumbra Embolectomy Aspiration System · Penumbra, Inc. · 2012K142870 · Penumbra Embolectomy Aspiration System [INDIGO Aspiration System] · Penumbra, Inc. · 2015×2: 2 generations cleared close together, K160533 (2016), K161523 (2016) ×2: 2 generations cleared close together, K180105 (2018), K180939 (2018) K193244 · Indigo Aspiration System – Lightning Aspiration Tubing · Penumbra, Inc. · 2020200020052010201520202025
  1. Root · 13 generations backK003410 Concentric Retriever, Model 90030Concentric Medical, Inc. · 2001 · Recalled
  2. 9 generations between
  3. 3 generations backK180105 Indigo Aspiration System - Penumbra Engine Pump, Indigo Aspiration…Penumbra, Inc. · 2018
  4. 2 generations backK180939 Indigo Aspiration System - Modified 110 Aspiration TubingPenumbra, Inc. · 2018
  5. 1 generation backK193244 Indigo Aspiration System – Lightning Aspiration TubingPenumbra, Inc. · 2020
  6. This deviceK210323 Indigo Aspiration System - Lightning Aspiration TubingPenumbra, Inc. · 2021
  7. Descendant · cites it directly · 8 of its ownK222358 Indigo Aspiration System - Lightning FlashPenumbra, Inc. · 2022
  8. Descendant · 2 generations on · 2 of its ownK240030 Indigo® Aspiration System - Lightning® FlashPenumbra, Inc. · 2024
  9. Descendant · 2 generations on · 1 of its ownK252956 Helo Thrombectomy SystemEndovascular Engineering, Inc. · 2025
  10. Descendant · 2 generations on · 1 of its ownK232679 Cleaner™ Pro Thrombectomy System; Cleaner™ Pro Aspiration Catheter…Argon Medical Devices, Inc. · 2024
  11. Descendant · cites it directly · 1 of its ownK223186 Indigo® Aspiration System – Lightning Bolt Aspiration TubingPenumbra, Inc. · 2023
Show all 13 generations
  1. Root · 13 generations backK003410 Concentric Retriever, Model 90030Concentric Medical, Inc. · 2001 · Recalled
  2. 12 generations backK030476 Modified Concentric Retriever, Model 90037Concentric Medical, Inc. · 2003 · Recalled
  3. 11 generations backK033736 Merci Retriever, Models 90065, 90066Concentric Medical, Inc. · 2004
  4. 10 generations backK072718 Penumbra SystemPenumbra, Inc. · 2007 · Recalled
  5. 9 generations backK100769 Penumbra System Separator Flex (026,032,041,054), Models PSF026…Penumbra, Inc. · 2010
  6. 8 generations backK113163 Penumbra System MaxPenumbra, Inc. · 2011
  7. 7 generations backK121917 Penumbra Embolectomy Aspiration SystemPenumbra, Inc. · 2012
  8. 6 generations backK142870 Penumbra Embolectomy Aspiration System [INDIGO Aspiration System]Penumbra, Inc. · 2015
  9. 5 generations backK160533 Penumbra Embolectomy Aspiration System (INDIGOTM Aspiration System)Penumbra, Inc. · 2016
  10. 4 generations backK161523 INDIGO Aspiration SystemPenumbra, Inc. · 2016
  11. 3 generations backK180105 Indigo Aspiration System - Penumbra Engine Pump, Indigo Aspiration…Penumbra, Inc. · 2018
  12. 2 generations backK180939 Indigo Aspiration System - Modified 110 Aspiration TubingPenumbra, Inc. · 2018
  13. 1 generation backK193244 Indigo Aspiration System – Lightning Aspiration TubingPenumbra, Inc. · 2020
  14. This deviceK210323 Indigo Aspiration System - Lightning Aspiration TubingPenumbra, Inc. · 2021

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2022: 12023: 12024: 42025: 22026: 3
2022high 4 (2024) · low 1 (2022)2026

Most influential descendants

Showing 5 of 11 · See all
  • K222358Indigo Aspiration System - Lightning FlashPenumbra, Inc. · 2022 · cites it directly8descendants
  • K240030Indigo® Aspiration System - Lightning® FlashPenumbra, Inc. · 2024 · 2 generations on2descendants
  • K252956Helo Thrombectomy SystemEndovascular Engineering, Inc. · 2025 · 2 generations on1descendant
  • K232679Cleaner™ Pro Thrombectomy System; Cleaner™ Pro Aspiration Catheter with Handpiece…Argon Medical Devices, Inc. · 2024 · 2 generations on1descendant
  • K223186Indigo® Aspiration System – Lightning Bolt Aspiration TubingPenumbra, Inc. · 2023 · cites it directly1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K003410Concentric Retriever, Model 90030Concentric Medical, Inc.20011
−12K030476Modified Concentric Retriever, Model 90037Concentric Medical, Inc.20032
−11K033736Merci Retriever, Models 90065, 90066Concentric Medical, Inc.2004—
−10K072718Penumbra SystemPenumbra, Inc.20071
−9K100769Penumbra System Separator Flex (026,032,041,054), Models PSF026, PSF032…Penumbra, Inc.2010—
−8K113163Penumbra System MaxPenumbra, Inc.2011—
−7K121917Penumbra Embolectomy Aspiration SystemPenumbra, Inc.2012—
−6K142870Penumbra Embolectomy Aspiration System [INDIGO Aspiration System]Penumbra, Inc.2015—
−5K160533Penumbra Embolectomy Aspiration System (INDIGOTM Aspiration System)Penumbra, Inc.2016—
−4K161523INDIGO Aspiration SystemPenumbra, Inc.2016—
−3K180105Indigo Aspiration System - Penumbra Engine Pump, Indigo Aspiration System -…Penumbra, Inc.2018—
−2K180939Indigo Aspiration System - Modified 110 Aspiration TubingPenumbra, Inc.2018—
−1K193244Indigo Aspiration System – Lightning Aspiration TubingPenumbra, Inc.2020—
0 (this device)K210323Indigo Aspiration System - Lightning Aspiration TubingPenumbra, Inc.2021—
+1K222358Indigo Aspiration System - Lightning FlashPenumbra, Inc.2022—
+2K240030Indigo® Aspiration System - Lightning® FlashPenumbra, Inc.2024—
+2K252956Helo Thrombectomy SystemEndovascular Engineering, Inc.2025—
+2K232679Cleaner™ Pro Thrombectomy System; Cleaner™ Pro Aspiration Catheter with…Argon Medical Devices, Inc.2024—
+1K223186Indigo® Aspiration System – Lightning Bolt Aspiration TubingPenumbra, Inc.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
202310
202440
202520
202630
FIG. 1 — Lineage of K210323, 2001–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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.

Planning a device in QEW? 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 QEW device

  1. #1 K213402 Triever24, Triever20score 28.6 · 5 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
*K193244Indigo Aspiration System – Lightning Aspiration Tubing
Summary page 4
…eter, Embolectomy Regulation Number: 21 CFR §870.5150 Product Code: QEW 4. Predicate and Reference Device Information Primary Predicate: K193244 – Indigo Aspiration System – Lightning Aspiration Tubing Reference Devices: K200771 – Indigo Aspiration System – Lightnin…
Penumbra, Inc.2020—
†K200771Indigo Aspiration System Lightning Aspiration TubingPenumbra, Inc.2020—
†K202821Indigo Aspiration System - Aspiration Catheter 12 and Separator 12Penumbra, Inc.2020—
†K180939Indigo Aspiration System - Modified 110 Aspiration TubingPenumbra, Inc.2018—

Also cleared against K193244: 2 other devices →

What descends from it? (11)

See all 11

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

NumberDeviceApplicantDecidedDescendants
K222358Indigo Aspiration System - Lightning FlashPenumbra, Inc.20228
K223186Indigo® Aspiration System – Lightning Bolt Aspiration TubingPenumbra, Inc.20231

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 20 years and passes through 2 companies; a new generation was cleared every 1.5 years on median.
  • 3 of the 15 ancestors have a recall of any class.
  • Of its descendants, K222358 (Penumbra, Inc., 2022) has gone furthest, with 8 descendants of its own.
  • 2 other devices also cite its predicate K193244.

How does its category compare?

All QEW devices

QEW Peripheral Mechanical Thrombectomy With Aspiration: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · QEW

14in 2025

2008: 22009: 22012: 12013: 22014: 22015: 42016: 42017: 22018: 142019: 82020: 162021: 112022: 122023: 232024: 142025: 142026 (partial year): 10
2007high 23 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QEW

58in 2025

2015: 88 days median2016: 63 days median2018: 61 days median2019: 51 days median2020: 105 days median2021: 60 days median2022: 140 days median2023: 102 days median2024: 65 days median2025: 58 days median2026 (partial year): 74 days median
2007high 140 (2022) · low 51 (2019)2026

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

Recalls per year · QEW

7in 2022

2022: 7, 7 Class I
2007high 7 (2022) · low 0 (2007)2026

Class I (7 since 2007) Class II/III not classified

Adverse event reports per year · QEW

207in 2025

2019: 332020: 1972021: 3222022: 1252023: 1652024: 1622025: 207
2007high 322 (2021) · low 0 (2007)2025

MAUDE reports naming product code QEW, 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
20070—00
20082—00
20092—00
20100—00
20110—00
20121—00
20132—00
20142—00
201548800
201646300
20172—00
2018146100
2019851033
2020161050197
202111600322
2022121407 (7)125
2023231020165
202414650162
202514580207
202610740—

What is it indicated for?

As part of the INDIGO Aspiration System, the INDIGO Aspiration Catheters and Separators are indicated for the removal of fresh, soft emboli and thrombi from vessels of the peripheral arterial and venous systems, and for the treatment of pulmonary embolism.

As part of the INDIGO Aspiration System, the INDIGO Sterile Aspiration Tubing is indicated to connect the INDIGO Aspiration Catheters to the Penumbra Aspiration Pump.

The Penumbra Aspiration Pump is indicated as a vacuum source for Penumbra Aspiration Systems.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K210323: Indigo Aspiration System - Lightning Aspiration Tubing.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K210323

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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