510(k) · Cleared
ClearedClickzip, Model U-100 Insulin Safety Syringe
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medical Device Manufacturer (Thailand), Ltd. · MEG Syringe, Antistick
Cleared on Jan 5, 2007 as substantially equivalent to K050134 (Formosa Medical Devices, Inc., 2005) and 1 other predicate after a 109-day review. Its family tree reaches back 2 generations to 1998.
- Decided
- Jan 5, 2007
- Review
- 109 days
- Class
- Class II
- Product code
- MEG
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 2 generations to K980580 (1998). 5 ancestors in all. No later device cites it as a predicate yet.
- Root · 2 generations backK980580 Becton Dickinson SyringesBd Becton Dickinson Vacutainer Systems Preanalytic · 1998
- 1 generation backK050134 Icc Insulin Safepro Safety SyringeFormosa Medical Devices, Inc. · 2005
- This deviceK062780 Clickzip, Model U-100 Insulin Safety SyringeMedical Device Manufacturer (Thailand), Ltd. · 2007
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K980580 | Becton Dickinson Syringes | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1998 | — |
| −1 | K050134 | Icc Insulin Safepro Safety Syringe | Formosa Medical Devices, Inc. | 2005 | — |
| 0 (this device) | K062780 | Clickzip, Model U-100 Insulin Safety Syringe | Medical Device Manufacturer (Thailand), Ltd. | 2007 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2001 | 1 | 0 |
| 2002 | 1 | 0 |
| 2005 | 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? (2)
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 |
|---|---|---|---|
| * | K050134 | Icc Insulin Safepro Safety SyringeSummary page 1…on Code: MEG Nominal Capacity: Iml. Insulin Unit: U-100 3. PREDICATE DEVICE * Icc Insulin SafePro Safety Syringe with 510(K) number K050134 * ClickZip T M Needle Retractable Safety Syringe with 5 10(K) number K051694 4. DEVICE DESCRIPTION The Clic… | 2005 |
| * | K051694 | Clickzip Needle Retractable Safety SyringeSummary page 1…TE DEVICE * Icc Insulin SafePro Safety Syringe with 510(K) number K050134 * ClickZip T M Needle Retractable Safety Syringe with 5 10(K) number K051694 4. DEVICE DESCRIPTION The ClickZip T M Needle Retractable Safety Syringe Insulin I ml. is sterile, single-use, dis… | 2005 |
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 9 years and passes through 3 companies; a new generation was cleared every 6.8 years on median.
- 1 of the 5 ancestors has a recall of any class.
- 2 other devices also cite its predicate K050134.
How does its category compare?
All MEG devicesMEG Syringe, Antistick: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, 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?
The ClickZip m Needle Retractable Safety Syringe Insulin 1 ml. with U-100 strength
insulin is to be used for subcutaneous injection of insulin into a patient and is intended to
prevent needle stick injuries.
In addition, when the syringe user breaks the plunger, re-use of the syringe is prevented.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K062780 · printed Nov 5, 2026
Cite this page
510(k) Report. “K062780: Clickzip, Model U-100 Insulin Safety Syringe.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K062780
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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