510(k) · Cleared
ClearedEXEL Disposable Syringe; EXEL Disposable Syringe with Needle; EXEL Disposable Syringe with Secure Touch® Safety Needle; EXEL Disposable Hypodermic Needle
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Exelint International, Co. · FMF Syringe, Piston
Cleared on Dec 12, 2025 as substantially equivalent to K232950 (Perfect Medical Industry (Vn) Co., Ltd., 2024) after a 246-day review. Its family tree reaches back 10 generations to 1977.
- Decided
- Dec 12, 2025
- Review
- 246 days
- Class
- Class II
- Product code
- FMF
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 10 generations to K771205 (1977). 21 ancestors in all. No later device cites it as a predicate yet.
- Root · 10 generations backK771205 Hypodermic SyringeTerumo America, Inc. · 1977
- 6 generations between
- 3 generations backK193526 Syringe with safety needle, Safety needleJiangsu Caina Medical Co.,Ltd · 2020
- 2 generations backK211329 Sterile Disposable Syringe with Saftey Needle, Sterile Disposable…Jiangsu Kangbao Medical Equipment Co., Ltd. · 2021
- 1 generation backK232950 Sterile Disposable Syringe, Sterile Disposable Syringe with needle…Perfect Medical Industry (Vn) Co., Ltd. · 2024
- This deviceK251089 EXEL Disposable Syringe; EXEL Disposable Syringe with Needle; EXEL…Exelint International, Co. · 2025
Show all 10 generations
- Root · 10 generations backK771205 Hypodermic SyringeTerumo America, Inc. · 1977
- 9 generations backK980181 Terumo Disposable Hypodermc SyringeTerumo Medical Corp. · 1998 · Recalled
- 8 generations backK023271 Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2002
- 7 generations backK052034 Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2005
- 6 generations backK063613 Modification to Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2006
- 5 generations backK083514 Terumo Syringe with/Without NeedleTerumo Europe N.V. · 2009
- 4 generations backK170651 Sterile Disposable Syringe with Safety Needle, Sterile Disposable…Yangzhou Medline Industry, Co., Ltd. · 2017
- 3 generations backK193526 Syringe with safety needle, Safety needleJiangsu Caina Medical Co.,Ltd · 2020
- 2 generations backK211329 Sterile Disposable Syringe with Saftey Needle, Sterile Disposable…Jiangsu Kangbao Medical Equipment Co., Ltd. · 2021
- 1 generation backK232950 Sterile Disposable Syringe, Sterile Disposable Syringe with needle…Perfect Medical Industry (Vn) Co., Ltd. · 2024
- This deviceK251089 EXEL Disposable Syringe; EXEL Disposable Syringe with Needle; EXEL…Exelint International, Co. · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K771205 | Hypodermic Syringe | Terumo America, Inc. | 1977 | — |
| −9 | K980181 | Terumo Disposable Hypodermc Syringe | Terumo Medical Corp. | 1998 | 1 |
| −8 | K023271 | Terumo Syringe with/Without Needle | Terumo Medical Corp. | 2002 | — |
| −7 | K052034 | Terumo Syringe with/Without Needle | Terumo Medical Corp. | 2005 | — |
| −6 | K063613 | Modification to Terumo Syringe with/Without Needle | Terumo Medical Corp. | 2006 | — |
| −5 | K083514 | Terumo Syringe with/Without Needle | Terumo Europe N.V. | 2009 | — |
| −4 | K170651 | Sterile Disposable Syringe with Safety Needle, Sterile Disposable Syringe with… | Yangzhou Medline Industry, Co., Ltd. | 2017 | — |
| −3 | K193526 | Syringe with safety needle, Safety needle | Jiangsu Caina Medical Co.,Ltd | 2020 | — |
| −2 | K211329 | Sterile Disposable Syringe with Saftey Needle, Sterile Disposable Syringe with… | Jiangsu Kangbao Medical Equipment Co., Ltd. | 2021 | — |
| −1 | K232950 | Sterile Disposable Syringe, Sterile Disposable Syringe with needle, Sterile… | Perfect Medical Industry (Vn) Co., Ltd. | 2024 | — |
| 0 (this device) | K251089 | EXEL Disposable Syringe; EXEL Disposable Syringe with Needle; EXEL Disposable… | Exelint International, Co. | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1977 | 1 | 0 |
| 1990 | 1 | 0 |
| 1993 | 1 | 0 |
| 1998 | 1 | 0 |
| 2001 | 1 | 0 |
| 2003 | 1 | 0 |
| 2004 | 1 | 0 |
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2012 | 1 | 0 |
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 K241821 Luer Lock Syringe with Safety Needle; Luer…score 16.2 · 8 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K232950 | Sterile Disposable Syringe, Sterile Disposable Syringe with needle, Sterile Disposable…Summary page 5…Regulatory Class: II Product Code(s): FMF, FMI, MEG Legally Marketed Predicate Devices Predicate #: K232950 Predicate Trade Name: Sterile Disposable Syringe Sterile Disposable S… | 2024 |
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 48 years and passes through 8 companies; a new generation was cleared every 2.7 years on median.
- 4 of the 21 ancestors have a recall of any class.
How does its category compare?
All FMF devicesFMF 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
2026 to Oct 25, outlined.
Median 510(k) review, days · FMF
114in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FMF
19in 2023
Class I (19 since 2007) Class II/III not classified
Adverse event reports per year · FMF
4,181in 2025
MAUDE reports naming product code FMF, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 23 | 90 | 6 | 674 |
| 2008 | 9 | 74 | 11 | 691 |
| 2009 | 14 | 94 | 15 | 913 |
| 2010 | 11 | 130 | 12 | 679 |
| 2011 | 16 | 109 | 3 | 186 |
| 2012 | 9 | 86 | 6 | 307 |
| 2013 | 12 | 154 | 1 | 326 |
| 2014 | 13 | 84 | 1 | 244 |
| 2015 | 11 | 87 | 2 | 273 |
| 2016 | 12 | 146 | 0 | 684 |
| 2017 | 13 | 135 | 3 | 1,858 |
| 2018 | 8 | 87 | 2 | 3,952 |
| 2019 | 11 | 146 | 1 | 5,863 |
| 2020 | 15 | 107 | 2 | 5,334 |
| 2021 | 20 | 175 | 1 | 5,874 |
| 2022 | 24 | 211 | 2 | 5,233 |
| 2023 | 22 | 173 | 19 (18) | 5,214 |
| 2024 | 14 | 130 | 0 | 5,122 |
| 2025 | 13 | 114 | 0 | 4,181 |
| 2026 | 9 | 239 | 2 (1) | — |
What is it indicated for?
These devices are intended to be used:
- to inject fluids into, or withdraw fluids from, the body.
- to administer and/or withdraw (aspirate) fluids/drugs.
These devices are intended for use by qualified healthcare professionals in a professional healthcare environment. These devices are intended for use in the general population, including both adult and pediatric patients of all age groups, as determined appropriate by the qualified healthcare professional using the device.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K251089 · printed Nov 4, 2026
Cite this page
510(k) Report. “K251089: EXEL Disposable Syringe; EXEL Disposable Syringe with Needle; EXEL Disposable Syringe with Secure Touch® Safety Needle; EXEL Disposable Hypodermic Needle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K251089
Report an extraction error
Are you the manufacturer?
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