510(k) Report

510(k) · Cleared

Cleared

Sterile syringes for single use with/without needle

K231729510(k) TraditionalCleared Sep 8, 202387-day reviewClass II21 CFR 880.5570

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

Wepon Medical Technology Co., Ltd. · FMI Needle, Hypodermic, Single Lumen

Cleared on Sep 8, 2023 as substantially equivalent to K112057 (Shanghai Kindly Enterprise Dev. Group Co.,, 2011) after an 87-day review. Its family tree reaches back 6 generations to 1993.

Decided
Sep 8, 2023
Review
87 days
Class
Class II
Product code
FMI
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K931367 (1993). 22 ancestors in all, the oldest K822083 (1982). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2007: 2 other ancestors2006: 1 other ancestor2003: 1 other ancestor2002: 1 other ancestor2001: 1 other ancestor2000: 2 other ancestors1999: 1 other ancestor1998: 1 other ancestor1997: 3 other ancestors1996: 1 other ancestor1995: 1 other ancestor1982: 1 other ancestorK931367 · 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. · 2008K110421 · Disposable Insulin Syringe · Wenzhou Wuzhou Import & Export Co., Ltd. · 2011K112057 · KDL Syringes and Needle · Shanghai Kindly Enterprise Dev. Group Co., · 201119801990200020102020
  1. Root · 6 generations backK931367 Vacutainer Brand Luer AdapterBd Becton Dickinson Vacutainer Systems Preanalytic · 1993
  2. 5 generations backK021475 BD Single Lumen Needle, Syringe and Blood Collection SetBd · 2002 · Recalled
  3. 4 generations backK070440 BD Hypoint NeedleBecton, Dickinson & CO · 2007
  4. 3 generations backK072739 Jierui Syringes and NeedlesShandong Weigao Group Medical Polymer Co., Ltd. · 2008
  5. 2 generations backK110421 Disposable Insulin SyringeWenzhou Wuzhou Import & Export Co., Ltd. · 2011
  6. 1 generation backK112057 KDL Syringes and NeedleShanghai Kindly Enterprise Dev. Group Co., · 2011
  7. This deviceK231729 Sterile syringes for single use with/without needleWepon Medical Technology Co., Ltd. · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K931367Vacutainer Brand Luer AdapterBd Becton Dickinson Vacutainer Systems Preanalytic1993—
−5K021475BD Single Lumen Needle, Syringe and Blood Collection SetBd20023
−4K070440BD Hypoint NeedleBecton, Dickinson & CO2007—
−3K072739Jierui Syringes and NeedlesShandong Weigao Group Medical Polymer Co., Ltd.2008—
−2K110421Disposable Insulin SyringeWenzhou Wuzhou Import & Export Co., Ltd.2011—
−1K112057KDL Syringes and NeedleShanghai Kindly Enterprise Dev. Group Co.,2011—
0 (this device)K231729Sterile syringes for single use with/without needleWepon Medical Technology Co., Ltd.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
199510
199610
199730
199810
199910
200020
200110
200210
200310
200610
200720
FIG. 1 — Lineage of K231729, 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 FMI? 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 FMI device

  1. #1 K252886 Pen Needlescore 14.5 · 4 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
*K112057KDL Syringes and Needle
Summary page 5
…1 |P a g e Product Code: FMI Premarket Notification: K112057 Manufacturer: Shanghai Kindly Enterprise Division Group Company V Device description The Sterile Syringes for Si…
Shanghai Kindly Enterprise Dev. Group Co.,2011—

Also cleared against K112057: 5 other devices →

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 30 years and passes through 7 companies; a new generation was cleared every 4.7 years on median.
  • 3 of the 22 ancestors have a recall of any class.
  • 5 other devices also cite its predicate K112057.

How does its category compare?

All FMI devices

FMI Needle, Hypodermic, Single Lumen: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · FMI

11in 2025

2007: 152008: 102009: 72010: 152011: 122012: 172013: 112014: 142015: 102016: 202017: 92018: 202019: 122020: 112021: 182022: 232023: 182024: 32025: 112026 (partial year): 12
2007high 23 (2022) · low 3 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FMI

141in 2025

2007: 71 days median2008: 85 days median2009: 177 days median2010: 119 days median2011: 113 days median2012: 107 days median2013: 87 days median2014: 155 days median2015: 89 days median2016: 217 days median2017: 253 days median2018: 176 days median2019: 186 days median2020: 263 days median2021: 143 days median2022: 189 days median2023: 112 days median2024: 90 days median2025: 141 days median2026 (partial year): 119 days median
2007high 263 (2020) · low 71 (2007)2026

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

Recalls per year · FMI

1in 2024

2007: 22008: 42009: 32010: 792011: 52012: 12013: 12014: 32015: 12017: 162019: 52020: 32021: 72023: 22024: 12026 (partial year): 1, 1 Class I
2007high 79 (2010) · low 0 (2016)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · FMI

2,424in 2025

2007: 2082008: 1772009: 2632010: 2492011: 2402012: 2152013: 2552014: 2872015: 5672016: 9412017: 1,5472018: 2,3982019: 4,8962020: 4,2452021: 4,5322022: 4,8852023: 4,9862024: 4,0532025: 2,424
2007high 4,986 (2023) · low 177 (2008)2025

MAUDE reports naming product code FMI, 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
200715712208
200810854177
200971773263
20101511979249
2011121135240
2012171071215
201311871255
2014141553287
201510891567
2016202170941
20179253161,547
20182017602,398
20191218654,896
20201126334,245
20211814374,532
20222318904,885
20231811224,986
202439014,053
20251114102,424
2026121191 (1)—

What is it indicated for?

The Sterile syringes for single use with/without needle is intended to be used for medical purposes to inject fluid into or

withdraw fluid from body.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K231729: Sterile syringes for single use with/without needle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K231729

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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