510(k) Report

510(k) · Cleared

Cleared

Disposable Insulin Syringe

K151949510(k) TraditionalCleared Oct 2, 201579-day reviewClass II21 CFR 880.5860

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

Jiangyin Caina Technology Co., Ltd. · FMF Syringe, Piston

Cleared on Oct 2, 2015 as substantially equivalent to K072739 (Shandong Weigao Group Medical Polymer Co., Ltd., 2008) after a 79-day review. Its family tree reaches back 4 generations to 1993. 6 later devices descend from it.

Decided
Oct 2, 2015
Review
79 days
Class
Class II
Product code
FMF
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K931367 (1993). 20 ancestors in all, the oldest K822083 (1982). 6 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2007: 2 other ancestors2006: 1 other ancestor2003: 1 other ancestor2001: 1 other ancestor2000: 2 other ancestors1999: 1 other ancestor1996: 1 other ancestor1982: 1 other ancestor2002: 1 other ancestor1998: 1 other ancestor1997: 3 other ancestors1995: 1 other ancestor2016: 1 descendant cleared2021: 1 descendant cleared2020: 2 descendants cleared2022: 1 descendant cleared2023: 1 descendant clearedReference device: K113091 · Syringes, With or without Needles · Jiangyin Caina Technology Co., Ltd. · 2011K931367 · Vacutainer Brand Luer Adapter · Bd Becton Dickinson Vacutainer Systems Preanalytic · 1993K021475 · BD Single Lumen Needle, Syringe and Blood Collection Set · Bd · 2002 · recalledK070440 · BD Hypoint Needle · Becton, Dickinson & CO · 2007K072739 · Jierui Syringes and Needles · Shandong Weigao Group Medical Polymer Co., Ltd. · 200819801990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 3 other ancestors3 generations back: 6 other ancestors4 generations back: 7 other ancestors 1 generation forward: 1 descendant2 generations forward: 3 descendants3 generations forward: 1 descendant4 generations forward: 1 descendant K072739 · Jierui Syringes and Needles · Shandong Weigao Group Medical Polymer Co., Ltd. · 2008K070440 · BD Hypoint Needle · Becton, Dickinson & CO · 2007K021475 · BD Single Lumen Needle, Syringe and Blood Collection Set · Bd · 2002 · recalledK931367 · Vacutainer Brand Luer Adapter · Bd Becton Dickinson Vacutainer Systems Preanalytic · 19930
  1. Root · 4 generations backK931367 Vacutainer Brand Luer AdapterBd Becton Dickinson Vacutainer Systems Preanalytic · 1993
  2. 3 generations backK021475 BD Single Lumen Needle, Syringe and Blood Collection SetBd · 2002 · Recalled
  3. 2 generations backK070440 BD Hypoint NeedleBecton, Dickinson & CO · 2007
  4. 1 generation backK072739 Jierui Syringes and NeedlesShandong Weigao Group Medical Polymer Co., Ltd. · 2008
  5. This deviceK151949 Disposable Insulin SyringeJiangyin Caina Technology Co., Ltd. · 2015
  6. Descendant · cites it directly · 5 of its ownK152808 U&U Insulin Syringe with/without Safety Retractable DeviceU&U Medical Technology Co, Ltd. · 2016
  7. Descendant · 2 generations on · 2 of its ownK202570 Insulin Syringe, Insulin Syringe with Safety RetractableJiangsu Micsafe Medical Technology Co., Ltd. · 2021
  8. Descendant · 3 generations on · 1 of its ownK220061 Safety Insulin SyringesBerpu Medical Technology Co., Ltd. · 2022
  9. Descendant · 4 generations on · 0 of its ownK230061 Insulin SyringeAnhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. · 2023
  10. Descendant · 2 generations on · 0 of its ownK191639 TK Insulin Syringe with/without Saftey Retractable DeviceAnhui Tiankang Medical Technology Co., Ltd. · 2020

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2016: 12020: 22021: 12022: 12023: 1
2016high 2 (2020) · low 0 (2017)2026

Most influential descendants

Showing 5 of 6 · See all
  • K152808U&U Insulin Syringe with/without Safety Retractable DeviceU&U Medical Technology Co, Ltd. · 2016 · cites it directly5descendants
  • K202570Insulin Syringe, Insulin Syringe with Safety RetractableJiangsu Micsafe Medical Technology Co., Ltd. · 2021 · 2 generations on2descendants
  • K220061Safety Insulin SyringesBerpu Medical Technology Co., Ltd. · 2022 · 3 generations on1descendant
  • K230061Insulin SyringeAnhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. · 2023 · 4 generations on0descendants
  • K191639TK Insulin Syringe with/without Saftey Retractable DeviceAnhui Tiankang Medical Technology Co., Ltd. · 2020 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K931367Vacutainer Brand Luer AdapterBd Becton Dickinson Vacutainer Systems Preanalytic1993—
−3K021475BD Single Lumen Needle, Syringe and Blood Collection SetBd20023
−2K070440BD Hypoint NeedleBecton, Dickinson & CO2007—
−1K072739Jierui Syringes and NeedlesShandong Weigao Group Medical Polymer Co., Ltd.2008—
0 (this device)K151949Disposable Insulin SyringeJiangyin Caina Technology Co., Ltd.2015—
+1K152808U&U Insulin Syringe with/without Safety Retractable DeviceU&U Medical Technology Co, Ltd.2016—
+2K202570Insulin Syringe, Insulin Syringe with Safety RetractableJiangsu Micsafe Medical Technology Co., Ltd.2021—
+3K220061Safety Insulin SyringesBerpu Medical Technology Co., Ltd.2022—
+4K230061Insulin SyringeAnhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.2023—
+2K191639TK Insulin Syringe with/without Saftey Retractable DeviceAnhui Tiankang Medical Technology Co., Ltd.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
199510
199610
199730
199810
199910
200020
200110
200210
200310
200610
200720

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
202020
202110
202210
202310
FIG. 1 — Lineage of K151949, 1993–2023Source: 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 FMF? 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 FMF device

  1. #1 K241821 Luer Lock Syringe with Safety Needle; Luer…score 16.1 · 8 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
*K072739Jierui Syringes and Needles
Summary page 6
…1ml 30G 3/8″, 1/2″, 5/16″or 5/8″ 5. Identification of Predicate Device 510(k) Number: K072739 Product Name: Sterile Insulin Syringe for single use with fixed needle Manufacturer: ShanDong Weigao Group Medical Poly…
Shandong Weigao Group Medical Polymer Co., Ltd.2008—
†K113091Syringes, With or without NeedlesJiangyin Caina Technology Co., Ltd.2011—

Also cleared against K072739: 10 other devices →

What descends from it? (6)

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

NumberDeviceApplicantDecidedDescendants
K152808U&U Insulin Syringe with/without Safety Retractable DeviceU&U Medical Technology Co, Ltd.20165

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 22 years and passes through 5 companies; a new generation was cleared every 7.5 years on median.
  • 3 of the 20 ancestors have a recall of any class.
  • Of its descendants, K152808 (U&U Medical Technology Co, Ltd., 2016) has gone furthest, with 5 descendants of its own.
  • 10 other devices also cite its predicate K072739.

How does its category compare?

All FMF devices

FMF Syringe, Piston: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · FMF

13in 2025

2007: 232008: 92009: 142010: 112011: 162012: 92013: 122014: 132015: 112016: 122017: 132018: 82019: 112020: 152021: 202022: 242023: 222024: 142025: 132026 (partial year): 9
2007high 24 (2022) · low 8 (2018)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FMF

114in 2025

2007: 90 days median2008: 74 days median2009: 94 days median2010: 130 days median2011: 109 days median2012: 86 days median2013: 154 days median2014: 84 days median2015: 87 days median2016: 146 days median2017: 135 days median2018: 87 days median2019: 146 days median2020: 107 days median2021: 175 days median2022: 211 days median2023: 173 days median2024: 130 days median2025: 114 days median2026 (partial year): 239 days median
2007high 239 (2026) · low 74 (2008)2026

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

Recalls per year · FMF

19in 2023

2007: 62008: 112009: 152010: 122011: 32012: 62013: 12014: 12015: 22017: 32018: 22019: 12020: 22021: 12022: 22023: 19, 18 Class I2026 (partial year): 2, 1 Class I
2007high 19 (2023) · low 0 (2016)2026

Class I (19 since 2007) Class II/III not classified

Adverse event reports per year · FMF

4,181in 2025

2007: 6742008: 6912009: 9132010: 6792011: 1862012: 3072013: 3262014: 2442015: 2732016: 6842017: 1,8582018: 3,9522019: 5,8632020: 5,3342021: 5,8742022: 5,2332023: 5,2142024: 5,1222025: 4,181
2007high 5,874 (2021) · low 186 (2011)2025

MAUDE reports naming product code FMF, 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
200723906674
200897411691
2009149415913
20101113012679
2011161093186
20129866307
2013121541326
201413841244
201511872273
2016121460684
20171313531,858
201888723,952
20191114615,863
20201510725,334
20212017515,874
20222421125,233
20232217319 (18)5,214
20241413005,122
20251311404,181
202692392 (1)—

What is it indicated for?

The disposable insulin syringe is intended for medical purposes for the manual aspiration of insulin, and for the injection of insulin into parts of the body below the surface skin.

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. “K151949: Disposable Insulin Syringe.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151949

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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