510(k) · Cleared
ClearedJeesung Safety Syringe and Single Use Needles
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Jeesung Medical Co., Ltd. · MEG Syringe, Antistick
Cleared on Jun 28, 2016 as substantially equivalent to K142435 (Sincere Medical Device Co., Ltd., 2015) after a 291-day review. Its family tree reaches back 2 generations to 2004. 1 later device descends from it.
- Decided
- Jun 28, 2016
- Review
- 291 days
- Class
- Class II
- Product code
- MEG
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K040545 (2004). 1 later device descends from it, 1 citing it directly.
- Root · 2 generations backK040545 Otter Safety SyringeOtter (China) Technology Co., Ltd. · 2004
- 1 generation backK142435 3S Safety Syringe with/without NeedleSincere Medical Device Co., Ltd. · 2015
- This deviceK152606 Jeesung Safety Syringe and Single Use NeedlesJeesung Medical Co., Ltd. · 2016
- Descendant · cites it directly · 0 of its ownK212518 Jeesung Safety Syringe and Single Use NeedlesJeesung Medical Co., Ltd. · 2022
Most influential descendants
Showing 1 of 1 · See all- K212518Jeesung Safety Syringe and Single Use NeedlesJeesung Medical Co., Ltd. · 2022 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K040545 | Otter Safety Syringe | Otter (China) Technology Co., Ltd. | 2004 | — |
| −1 | K142435 | 3S Safety Syringe with/without Needle | Sincere Medical Device Co., Ltd. | 2015 | — |
| 0 (this device) | K152606 | Jeesung Safety Syringe and Single Use Needles | Jeesung Medical Co., Ltd. | 2016 | — |
| +1 | K212518 | Jeesung Safety Syringe and Single Use Needles | Jeesung Medical Co., Ltd. | 2022 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2022 | 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 MEG? 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 MEG device
- #1 K192551 1ml Luer Slip or Luer Lock Syringe, Syringe…score 19.6 · 7 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 |
|---|---|---|---|
| * | K142435 | 3S Safety Syringe with/without NeedleSummary page 4…tion Name: Piston Syringe 4) Product Code: MEG 5) Regulation Number: 880.5860 6) Class of device: Class II 7) Panel: General Hospital 3. Predicate Device K142435 3S Safety Syringe with/without Needle 4. Device Description Jeesung Safety Syringe and Single Use Needles is an integrated ne… | 2015 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K212518 | Jeesung Safety Syringe and Single Use Needles | 2022 | 0 |
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 12 years and passes through 3 companies; a new generation was cleared every 10.8 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K212518 (Jeesung Medical Co., Ltd., 2022) has gone furthest, with 0 descendants of its own.
How does its category compare?
All MEG devicesMEG Syringe, Antistick: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.
FDA decisions per year · MEG
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MEG
229in 2023
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MEG
1in 2024
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · MEG
148in 2025
MAUDE reports naming product code MEG, 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 | 8 | 100 | 0 | 21 |
| 2008 | 4 | 145 | 1 | 20 |
| 2009 | 2 | — | 0 | 26 |
| 2010 | 2 | — | 1 | 34 |
| 2011 | 5 | 113 | 0 | 34 |
| 2012 | 5 | 109 | 0 | 22 |
| 2013 | 1 | — | 5 | 27 |
| 2014 | 5 | 153 | 0 | 36 |
| 2015 | 7 | 253 | 1 | 51 |
| 2016 | 3 | 179 | 0 | 94 |
| 2017 | 3 | 130 | 0 | 181 |
| 2018 | 1 | — | 0 | 269 |
| 2019 | 4 | 249 | 0 | 497 |
| 2020 | 4 | 296 | 0 | 353 |
| 2021 | 5 | 152 | 0 | 541 |
| 2022 | 13 | 216 | 0 | 170 |
| 2023 | 5 | 229 | 0 | 120 |
| 2024 | 0 | — | 1 (1) | 112 |
| 2025 | 1 | — | 0 | 148 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
Jeesung safety syringe and single use needles is a sterile, single-use, disposable and non-reusable, manual retractable safety syringe intended for injection of fluids into the body, while reducing the risk of sharps injuries and the potential for syringe reuse.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K152606 · printed Nov 6, 2026
Cite this page
510(k) Report. “K152606: Jeesung Safety Syringe and Single Use Needles.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K152606
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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