510(k) Report

510(k) · Cleared

Cleared

Verisafe Safety Retractable Insulin Syringes

K250192510(k) TraditionalCleared Dec 10, 2025321-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 Dec 10, 2025 as substantially equivalent to K231792 (Promisemed Hangzhou Meditech Co., Ltd., 2023) after a 321-day review. Its family tree reaches back 10 generations to 1993.

Decided
Dec 10, 2025
Review
321 days
Class
Class II
Product code
FMF
Recalls
None
Predicates
1

Its longest line of descent runs back 10 generations to K931367 (1993). 26 ancestors in all, the oldest K822083 (1982). No later device cites it as a predicate yet.

  1. Root · 10 generations backK931367 Vacutainer Brand Luer AdapterBd Becton Dickinson Vacutainer Systems Preanalytic · 1993
  2. 6 generations between
  3. 3 generations backK211242 Promisemed Sterile Hypodermic Syringes, Verifine Sterile Hypodermic…Promisemed Hangzhou Meditech Co., Ltd. · 2021
  4. 2 generations backK213560 Verifine Safety Syringe with Fixed NeedlePromisemed Hangzhou Meditech Co., Ltd. · 2022
  5. 1 generation backK231792 VeriSafe Safety sterile syringesPromisemed Hangzhou Meditech Co., Ltd. · 2023
  6. This deviceK250192 Verisafe Safety Retractable Insulin SyringesPromisemed Hangzhou Meditech Co., Ltd. · 2025
Show all 10 generations
  1. Root · 10 generations backK931367 Vacutainer Brand Luer AdapterBd Becton Dickinson Vacutainer Systems Preanalytic · 1993
  2. 9 generations backK021475 BD Single Lumen Needle, Syringe and Blood Collection SetBd · 2002 · Recalled
  3. 8 generations backK070440 BD Hypoint NeedleBecton, Dickinson & CO · 2007
  4. 7 generations backK072739 Jierui Syringes and NeedlesShandong Weigao Group Medical Polymer Co., Ltd. · 2008
  5. 6 generations backK110421 Disposable Insulin SyringeWenzhou Wuzhou Import & Export Co., Ltd. · 2011
  6. 5 generations backK112057 KDL Syringes and NeedleShanghai Kindly Enterprise Dev. Group Co., · 2011
  7. 4 generations backK153537 Sol-M Insulin Syringe, Sol-M TB SyringeSol-Millennium Medical, Inc. · 2016
  8. 3 generations backK211242 Promisemed Sterile Hypodermic Syringes, Verifine Sterile Hypodermic…Promisemed Hangzhou Meditech Co., Ltd. · 2021
  9. 2 generations backK213560 Verifine Safety Syringe with Fixed NeedlePromisemed Hangzhou Meditech Co., Ltd. · 2022
  10. 1 generation backK231792 VeriSafe Safety sterile syringesPromisemed Hangzhou Meditech Co., Ltd. · 2023
  11. This deviceK250192 Verisafe Safety Retractable Insulin SyringesPromisemed Hangzhou Meditech Co., Ltd. · 2025
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K931367Vacutainer Brand Luer AdapterBd Becton Dickinson Vacutainer Systems Preanalytic1993—
−9K021475BD Single Lumen Needle, Syringe and Blood Collection SetBd20023
−8K070440BD Hypoint NeedleBecton, Dickinson & CO2007—
−7K072739Jierui Syringes and NeedlesShandong Weigao Group Medical Polymer Co., Ltd.2008—
−6K110421Disposable Insulin SyringeWenzhou Wuzhou Import & Export Co., Ltd.2011—
−5K112057KDL Syringes and NeedleShanghai Kindly Enterprise Dev. Group Co.,2011—
−4K153537Sol-M Insulin Syringe, Sol-M TB SyringeSol-Millennium Medical, Inc.2016—
−3K211242Promisemed Sterile Hypodermic Syringes, Verifine Sterile Hypodermic SyringesPromisemed Hangzhou Meditech Co., Ltd.2021—
−2K213560Verifine Safety Syringe with Fixed NeedlePromisemed Hangzhou Meditech Co., Ltd.2022—
−1K231792VeriSafe Safety sterile syringesPromisemed Hangzhou Meditech Co., Ltd.2023—
0 (this device)K250192Verisafe 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
FIG. 1 — Lineage of K250192, 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 16.2 · 8 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
*K231792VeriSafe Safety sterile syringes
Summary page 5
…ode FMF, MEG 3. Legally Marketed Predicate Device [21 CFR 807.92 (a) (3)] Predicate Name VeriSafe Safety sterile syringes 510(k) Number K231792 Product Code FMF, MEG Reference Devices No reference devices were used in this submission. 4. Device Descript…
Promisemed Hangzhou Meditech Co., Ltd.2023—

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 32 years and passes through 8 companies; a new generation was cleared every 3.1 years on median.
  • 3 of the 26 ancestors have a recall of any class.

How does its category compare?

All FMF devices

FMF Syringe, Piston: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, 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?

Verisafe Safety Retractable Insulin Syringes are intended for aspiration and subcutaneous injection of insulin. After injection, the needle can be retracted directly from the patient's skin into the syringe barrel to avoid exposure to a contaminated needle, thereby minimizing accidental needle stick injuries.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K250192: Verisafe Safety Retractable Insulin Syringes.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K250192

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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