510(k) Report

510(k) · Cleared

Cleared

Promisemed Sterile Hypodermic Syringes, Verifine Sterile Hypodermic Syringes

K211242510(k) TraditionalCleared Sep 9, 2021136-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

Promisemed Hangzhou Meditech Co., Ltd. · FMF Syringe, Piston

Cleared on Sep 9, 2021 as substantially equivalent to K153537 (Sol-Millennium Medical, Inc., 2016) after a 136-day review. Its family tree reaches back 7 generations to 1993. 3 later devices descend from it.

Decided
Sep 9, 2021
Review
136 days
Class
Class II
Product code
FMF
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K931367 (1993). 23 ancestors in all, the oldest K822083 (1982). 3 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 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 ancestor2022: 1 descendant cleared2023: 1 descendant cleared2025: 1 descendant clearedK931367 · 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., · 2011K153537 · Sol-M Insulin Syringe, Sol-M TB Syringe · Sol-Millennium Medical, Inc. · 201619801990200020102020
  1. Root · 7 generations backK931367 Vacutainer Brand Luer AdapterBd Becton Dickinson Vacutainer Systems Preanalytic · 1993
  2. 6 generations backK021475 BD Single Lumen Needle, Syringe and Blood Collection SetBd · 2002 · Recalled
  3. 5 generations backK070440 BD Hypoint NeedleBecton, Dickinson & CO · 2007
  4. 4 generations backK072739 Jierui Syringes and NeedlesShandong Weigao Group Medical Polymer Co., Ltd. · 2008
  5. 3 generations backK110421 Disposable Insulin SyringeWenzhou Wuzhou Import & Export Co., Ltd. · 2011
  6. 2 generations backK112057 KDL Syringes and NeedleShanghai Kindly Enterprise Dev. Group Co., · 2011
  7. 1 generation backK153537 Sol-M Insulin Syringe, Sol-M TB SyringeSol-Millennium Medical, Inc. · 2016
  8. This deviceK211242 Promisemed Sterile Hypodermic Syringes, Verifine Sterile Hypodermic…Promisemed Hangzhou Meditech Co., Ltd. · 2021
  9. Descendant · cites it directly · 2 of its ownK213560 Verifine Safety Syringe with Fixed NeedlePromisemed Hangzhou Meditech Co., Ltd. · 2022
  10. Descendant · 2 generations on · 1 of its ownK231792 VeriSafe Safety sterile syringesPromisemed Hangzhou Meditech Co., Ltd. · 2023
  11. Descendant · 3 generations on · 0 of its ownK250192 Verisafe Safety Retractable Insulin SyringesPromisemed Hangzhou Meditech Co., Ltd. · 2025

Most influential descendants

Showing 3 of 3 · See all
  • K213560Verifine Safety Syringe with Fixed NeedlePromisemed Hangzhou Meditech Co., Ltd. · 2022 · cites it directly2descendants
  • K231792VeriSafe Safety sterile syringesPromisemed Hangzhou Meditech Co., Ltd. · 2023 · 2 generations on1descendant
  • K250192Verisafe Safety Retractable Insulin SyringesPromisemed Hangzhou Meditech Co., Ltd. · 2025 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K931367Vacutainer Brand Luer AdapterBd Becton Dickinson Vacutainer Systems Preanalytic1993—
−6K021475BD Single Lumen Needle, Syringe and Blood Collection SetBd20023
−5K070440BD Hypoint NeedleBecton, Dickinson & CO2007—
−4K072739Jierui Syringes and NeedlesShandong Weigao Group Medical Polymer Co., Ltd.2008—
−3K110421Disposable Insulin SyringeWenzhou Wuzhou Import & Export Co., Ltd.2011—
−2K112057KDL Syringes and NeedleShanghai Kindly Enterprise Dev. Group Co.,2011—
−1K153537Sol-M Insulin Syringe, Sol-M TB SyringeSol-Millennium Medical, Inc.2016—
0 (this device)K211242Promisemed Sterile Hypodermic Syringes, Verifine Sterile Hypodermic SyringesPromisemed Hangzhou Meditech Co., Ltd.2021—
+1K213560Verifine Safety Syringe with Fixed NeedlePromisemed Hangzhou Meditech Co., Ltd.2022—
+2K231792VeriSafe Safety sterile syringesPromisemed Hangzhou Meditech Co., Ltd.2023—
+3K250192Verisafe Safety Retractable Insulin SyringesPromisemed Hangzhou Meditech Co., Ltd.2025—

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
202210
202310
202510
FIG. 1 — Lineage of K211242, 1993–2025Source: 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
*K153537Sol-M Insulin Syringe, Sol-M TB Syringe
Summary page 4
…Classification name: Syringe, Piston Regulation Number: 21 CFR 880.5860 Device Class: Class II Product Code: FMF 4 Identification of Predicate Device K153537: Sol-M TB Syringe Page 1 of 7 Sterile Hypodermic Syringes…
Sol-Millennium Medical, Inc.2016—

Also cleared against K153537: 1 other device →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K213560Verifine Safety Syringe with Fixed NeedlePromisemed Hangzhou Meditech Co., Ltd.20222

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 28 years and passes through 8 companies; a new generation was cleared every 4.5 years on median.
  • 3 of the 23 ancestors have a recall of any class.
  • Of its descendants, K213560 (Promisemed Hangzhou Meditech Co., Ltd., 2022) has gone furthest, with 2 descendants of its own.
  • 1 other device also cites its predicate K153537.

How does its category compare?

All FMF devices

FMF Syringe, Piston: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, 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?

It is intended to be used for medical purposes to inject fluids into or withdraw fluids from the body.

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. “K211242: Promisemed Sterile Hypodermic Syringes, Verifine Sterile Hypodermic Syringes.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K211242

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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