510(k) Report

510(k) · Cleared

Cleared

Bendit2.7 Steerable Microcatheter

K200582510(k) TraditionalCleared Jun 25, 2020111-day reviewClass II21 CFR 870.1210

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

Bend IT Technologies, Ltd. · KRA Catheter, Continuous Flush

Cleared on Jun 25, 2020 as substantially equivalent to K190126 (Bend IT Technologies, Ltd., 2019) after a 111-day review. Its family tree reaches back 9 generations to 1996. 1 later device descends from it.

Decided
Jun 25, 2020
Review
111 days
Class
Class II
Product code
KRA
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K960806 (1996). 14 ancestors in all, the oldest K925813 (1994). 1 later device descends from it, 1 citing it directly.

  1. Root · 9 generations backK960806 Turbo TrackerTarget Therapeutics · 1996
  2. 5 generations between
  3. 3 generations backK072526 Micrus Courier Enzo Microcatheter 0.0190Micrus Endovascular Corporation · 2007
  4. 2 generations backK161921 SwiftNINJA MicrocatheterMerit Medical Systems, Inc. · 2016
  5. 1 generation backK190126 Bendit2.7 Steerable MicrocatheterBend IT Technologies, Ltd. · 2019
  6. This deviceK200582 Bendit2.7 Steerable MicrocatheterBend IT Technologies, Ltd. · 2020
  7. Descendant · cites it directly · 0 of its ownK211110 Agile Devices Angler Steerable, Deflectable MicrocatheterAgile Devices, Inc. · 2022
Show all 9 generations
  1. Root · 9 generations backK960806 Turbo TrackerTarget Therapeutics · 1996
  2. 8 generations backK994155 Excelsior 1018 MicrocatheterBoston Scientific, Target · 2000
  3. 7 generations backK013789 Excelsior SL-10 Microcatheter, Models 168581, 168381, 168181, 168189Boston Scientific, Target · 2001 · Recalled
  4. 6 generations backK042568 Excelsior 1018 and SL-10 MicrocathetersBoston Scientific Corp · 2004 · Recalled
  5. 5 generations backK061963 Micrus Microcatheter Courier Pre-Shaped, Models MPS170045-00…Micrus Endovascular Corporation · 2006
  6. 4 generations backK070456 Micrus Courier Enzo Microcatheter 0.017Micrus Endovascular Corporation · 2007
  7. 3 generations backK072526 Micrus Courier Enzo Microcatheter 0.0190Micrus Endovascular Corporation · 2007
  8. 2 generations backK161921 SwiftNINJA MicrocatheterMerit Medical Systems, Inc. · 2016
  9. 1 generation backK190126 Bendit2.7 Steerable MicrocatheterBend IT Technologies, Ltd. · 2019
  10. This deviceK200582 Bendit2.7 Steerable MicrocatheterBend IT Technologies, Ltd. · 2020

Most influential descendants

Showing 1 of 1 · See all
  • K211110Agile Devices Angler Steerable, Deflectable MicrocatheterAgile Devices, Inc. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K960806Turbo TrackerTarget Therapeutics1996—
−8K994155Excelsior 1018 MicrocatheterBoston Scientific, Target2000—
−7K013789Excelsior SL-10 Microcatheter, Models 168581, 168381, 168181, 168189Boston Scientific, Target20012
−6K042568Excelsior 1018 and SL-10 MicrocathetersBoston Scientific Corp20047
−5K061963Micrus Microcatheter Courier Pre-Shaped, Models MPS170045-00, MPS170090-00…Micrus Endovascular Corporation2006—
−4K070456Micrus Courier Enzo Microcatheter 0.017Micrus Endovascular Corporation2007—
−3K072526Micrus Courier Enzo Microcatheter 0.0190Micrus Endovascular Corporation2007—
−2K161921SwiftNINJA MicrocatheterMerit Medical Systems, Inc.2016—
−1K190126Bendit2.7 Steerable MicrocatheterBend IT Technologies, Ltd.2019—
0 (this device)K200582Bendit2.7 Steerable MicrocatheterBend IT Technologies, Ltd.2020—
+1K211110Agile Devices Angler Steerable, Deflectable MicrocatheterAgile Devices, Inc.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199710
200310
200610
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K200582, 1996–2022Source: 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.

Planning a device in KRA? 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 KRA device

  1. #1 K253509 TriSalus TriNav Advance Infusion Systemscore 14.4 · 9 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
*K190126Bendit2.7 Steerable Microcatheter
Summary page 4
…KRA Review Panel: Cardiovascular Class: II E. Predicate Device: Bendit2.7™ Steerable Microcatheter, K190126 F. Summary Device Description: The Bendit2.7™ is a steerable microcatheter with a steerable distal tip. The tip’s deflec…
Bend IT Technologies, Ltd.2019—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K211110Agile Devices Angler Steerable, Deflectable MicrocatheterAgile Devices, Inc.20220

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 24 years and passes through 6 companies; a new generation was cleared every 1.8 years on median.
  • 4 of the 14 ancestors have a recall of any class.
  • Of its descendants, K211110 (Agile Devices, Inc., 2022) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KRA devices

KRA Catheter, Continuous Flush: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · KRA

1in 2025

2007: 52008: 72009: 52010: 22011: 22012: 32013: 32014: 42016: 82017: 42018: 42019: 42020: 62021: 62022: 62023: 72025: 12026 (partial year): 5
2007high 8 (2016) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KRA

63in 2023

2007: 44 days median2008: 144 days median2009: 69 days median2012: 29 days median2013: 126 days median2014: 61 days median2016: 122 days median2017: 166 days median2018: 178 days median2019: 133 days median2020: 29 days median2021: 108 days median2022: 228 days median2023: 63 days median2026 (partial year): 268 days median
2007high 268 (2026) · low 29 (2012)2026

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

Recalls per year · KRA

41so far in 2026, the most since 2007

2007: 22008: 62009: 82010: 262011: 32012: 32013: 22014: 3, 2 Class I2015: 12016: 3, 1 Class I2019: 4, 4 Class I2020: 12023: 22026 (partial year): 41
2007high 41 (2026) · low 0 (2017)2026

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

Adverse event reports per year · KRA

980in 2025

2007: 1182008: 1172009: 1872010: 3552011: 2392012: 2172013: 2092014: 2762015: 3392016: 4182017: 5382018: 4342019: 4182020: 3812021: 4402022: 5432023: 8292024: 9422025: 980
2007high 980 (2025) · low 117 (2008)2025

MAUDE reports naming product code KRA, 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
20075442118
200871446117
20095698187
20102—26355
20112—3239
20123293217
201331262209
20144613 (2)276
20150—1339
201681223 (1)418
201741660538
201841780434
201941334 (4)418
20206291381
202161080440
202262280543
20237632829
20240—0942
20251—0980
2026526841—

What is it indicated for?

The Bendit2.7™ Steerable Microcatheter is intended for general intravascular use in the peripheral vasculature. The microcatheter can be used for the delivery of diagnostic, embolic, or therapeutic materials into the vasculature.

The Bendit2.7™ is not intended to be used in intracranial or coronary vessels.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K200582: Bendit2.7 Steerable Microcatheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K200582

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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