510(k) Report

510(k) · Cleared

Cleared

Luer Lock Syringe with Safety Needle; Luer Lock Syringe with Exchangeable Needle; Luer Lock Syringe with Blunt Fill Needle

K241821510(k) TraditionalCleared Sep 20, 202488-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

Sol-Millennium Medical, Inc. · FMF Syringe, Piston

Cleared on Sep 20, 2024 as substantially equivalent to K221247 (Jiangsu Kangbao Medical Equipment Co., Ltd., 2022) after an 88-day review. Its family tree reaches back 8 generations to 1977. 2 later devices descend from it.

Decided
Sep 20, 2024
Review
88 days
Class
Class II
Product code
FMF
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K771205 (1977). 19 ancestors in all. 2 later devices descend from it, 2 citing it directly.

  1. Root · 8 generations backK771205 Hypodermic SyringeTerumo America, Inc. · 1977
  2. 7 generations backK980181 Terumo Disposable Hypodermc SyringeTerumo Medical Corp. · 1998 · Recalled
  3. 6 generations backK023271 Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2002
  4. 5 generations backK052034 Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2005
  5. 4 generations backK063613 Modification to Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2006
  6. 3 generations backK083514 Terumo Syringe with/Without NeedleTerumo Europe N.V. · 2009
  7. 2 generations backK170651 Sterile Disposable Syringe with Safety Needle, Sterile Disposable…Yangzhou Medline Industry, Co., Ltd. · 2017
  8. 1 generation backK221247 Sterile Disposable Syringe with Safety Needle, Sterile Disposable…Jiangsu Kangbao Medical Equipment Co., Ltd. · 2022
  9. This deviceK241821 Luer Lock Syringe with Safety Needle; Luer Lock Syringe with…Sol-Millennium Medical, Inc. · 2024
  10. Descendant · cites it directly · 0 of its ownK252184 SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc. · 2026
  11. Descendant · cites it directly · 0 of its ownK253110 Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc. · 2026

Most influential descendants

Showing 2 of 2 · See all
  • K252184SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc. · 2026 · cites it directly0descendants
  • K253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K771205Hypodermic SyringeTerumo America, Inc.1977—
−7K980181Terumo Disposable Hypodermc SyringeTerumo Medical Corp.19981
−6K023271Terumo Syringe with/Without NeedleTerumo Medical Corp.2002—
−5K052034Terumo Syringe with/Without NeedleTerumo Medical Corp.2005—
−4K063613Modification to Terumo Syringe with/Without NeedleTerumo Medical Corp.2006—
−3K083514Terumo Syringe with/Without NeedleTerumo Europe N.V.2009—
−2K170651Sterile Disposable Syringe with Safety Needle, Sterile Disposable Syringe with…Yangzhou Medline Industry, Co., Ltd.2017—
−1K221247Sterile Disposable Syringe with Safety Needle, Sterile Disposable Syringe with…Jiangsu Kangbao Medical Equipment Co., Ltd.2022—
0 (this device)K241821Luer Lock Syringe with Safety Needle; Luer Lock Syringe with Exchangeable…Sol-Millennium Medical, Inc.2024—
+1K252184SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc.2026—
+1K253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197710
199010
199310
199810
200110
200310
200410
200510
200610
200710
201210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202620
FIG. 1 — Lineage of K241821, 1977–2026Source: 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 K262581 GraftGun Universal Graft Delivery System (GDS®)score 15.5 · 13 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
*K221247Sterile Disposable Syringe with Safety Needle, Sterile Disposable Syringe with Needle…
Summary page 6
…cation Name: Needle, Hypodermic, Single Lumen Classification: II Product Code: FMI Regulation Number: 21CFR 880.5570 Review Panel: General Hospital 4. Predicate device K221247 Sterile Disposable Syringe with Safety Needle, Sterile Disposable Syringe with Needle, Sterile Disposable Safety Needle, Sterile…
Jiangsu Kangbao Medical Equipment Co., Ltd.2022—

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K252184SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc.20260
K253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc.20260

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 47 years and passes through 6 companies; a new generation was cleared every 4.7 years on median.
  • 4 of the 19 ancestors have a recall of any class.
  • Of its descendants, K252184 (Sol-Millennium Medical, Inc., 2026) has gone furthest, with 0 descendants of its own.

How does its category compare?

All FMF devices

FMF Syringe, Piston: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, 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 Luer Lock Syringe with Exchangeable Needle is used to inject medicines and vaccines into, or withdraw fluids from, the body.

The Luer Lock Syringe with Safety Needle is used to inject fluids into, or withdraw fluids from, the body. The safety mechanism covers the needle after use. In the activated position, the protective arm guards against accidental needle stick during normal handling and disposal of the used needle/syringe combination.

The Luer Lock Syringe with Blunt Fill Needle is used for aspiration from multi-dose medicine vials.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K241821: Luer Lock Syringe with Safety Needle; Luer Lock Syringe with Exchangeable Needle; Luer Lock Syringe with Blunt Fill Needle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K241821

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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