510(k) Report

510(k) · Cleared

Cleared

injeTAK Adjustable Tip Needle (DIS199; DIS201)

K241523510(k) SpecialCleared Aug 27, 202490-day reviewClass II21 CFR 876.1500

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

Laborie Medical Technologies, Corp. · FBK Endoscopic Injection Needle, Gastroenterology-Urology

Cleared on Aug 27, 2024 as substantially equivalent to K090830 (Laborie Medical Technologies, Ltd., 2009) after a 90-day review. Its family tree reaches back 6 generations to 1982.

Decided
Aug 27, 2024
Review
90 days
Class
Class II
Product code
FBK
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K820973 (1982). 11 ancestors in all, the oldest K812057 (1981). No later device cites it as a predicate yet.

  1. Root · 6 generations backK820973 Endoscopic Injection NeedleMill-Rose Laboratory · 1982
  2. 5 generations backK960519 Martech Endoscopic Injection NeedleMartech Medical Products, Inc. · 1996
  3. 4 generations backK982890 Advanced Uroscience Injection NeedleAdvanced Uroscience, Inc. · 1998
  4. 3 generations backK990996 Genyx Medical Injection NeedleGenyx Medical, Inc. · 1999
  5. 2 generations backK022484 Cook Injection NeedleCook Urological, Inc. · 2002
  6. 1 generation backK090830 Laborie Injetak Adjustable Tip Needle, Flexible Tip and Ridgid TipLaborie Medical Technologies, Ltd. · 2009 · Recalled
  7. This deviceK241523 injeTAK Adjustable Tip Needle (DIS199; DIS201)Laborie Medical Technologies, Corp. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K820973Endoscopic Injection NeedleMill-Rose Laboratory1982—
−5K960519Martech Endoscopic Injection NeedleMartech Medical Products, Inc.1996—
−4K982890Advanced Uroscience Injection NeedleAdvanced Uroscience, Inc.1998—
−3K990996Genyx Medical Injection NeedleGenyx Medical, Inc.1999—
−2K022484Cook Injection NeedleCook Urological, Inc.2002—
−1K090830Laborie Injetak Adjustable Tip Needle, Flexible Tip and Ridgid TipLaborie Medical Technologies, Ltd.20091
0 (this device)K241523injeTAK Adjustable Tip Needle (DIS199; DIS201)Laborie Medical Technologies, Corp.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198110
198410
199310
199810
200510
FIG. 1 — Lineage of K241523, 1982–2024Source: 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 FBK? 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 FBK device

  1. #1 K253598 InjecSURE Injection Systemscore 12.9 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K090830Laborie Injetak Adjustable Tip Needle, Flexible Tip and Ridgid Tip
Summary page 5
…1500 Product Code(s) FBK, N/A | Legally Marketed Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K090830 injeTAK Adjustable Tip Needle FBK Device Description Summary 21 CFR 807.92(a)(4) The injeTAK Adjustable Tip Needles (injeTAK Nee…
Laborie Medical Technologies, Ltd.20091

Also cleared against K090830: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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 42 years and passes through 7 companies; a new generation was cleared every 6.7 years on median.
  • 1 of the 11 ancestors has a recall of any class.
  • 1 other device also cites its predicate K090830.

How does its category compare?

All FBK devices

FBK Endoscopic Injection Needle, Gastroenterology-Urology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · FBK

3in 2025

2008: 12009: 42011: 12012: 22014: 22015: 32016: 22017: 32018: 22019: 12020: 22021: 12022: 62023: 32024: 42025: 32026 (partial year): 2
2007high 6 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FBK

155in 2025

2009: 101 days median2015: 103 days median2017: 51 days median2022: 213 days median2023: 177 days median2024: 192 days median2025: 155 days median
2007high 213 (2022) · low 51 (2017)2026

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

Recalls per year · FBK

9in 2024

2016: 12021: 202022: 82023: 12024: 92026 (partial year): 1
2007high 20 (2021) · low 0 (2007)2026

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

Adverse event reports per year · FBK

81in 2025

2007: 32008: 222009: 122010: 122011: 22012: 22013: 32014: 92015: 42016: 182017: 272018: 92019: 62020: 252021: 342022: 802023: 602024: 942025: 81
2007high 94 (2024) · low 2 (2011)2025

MAUDE reports naming product code FBK, 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—03
20081—022
20094101012
20100—012
20111—02
20122—02
20130—03
20142—09
2015310304
20162—118
2017351027
20182—09
20191—06
20202—025
20211—2034
20226213880
20233177160
20244192994
20253155081
20262—1—

What is it indicated for?

The injeTAK Adjustable Tip Needles are intended to be used to deliver a variety of legally marketed drugs into tissues or structures during cystoscopic procedures. They are provided sterile for single use only.

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. “K241523: injeTAK Adjustable Tip Needle (DIS199; DIS201).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K241523

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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