510(k) Report

510(k) · Cleared

Cleared

Insulin Syringe, Insulin Syringe with Safety Retractable

K202570510(k) TraditionalCleared Jul 2, 2021301-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

Jiangsu Micsafe Medical Technology Co., Ltd. · MEG Syringe, Antistick

Cleared on Jul 2, 2021 as substantially equivalent to K152808 (U&U Medical Technology Co, Ltd., 2016) after a 301-day review. Its family tree reaches back 6 generations to 2000. 2 later devices descend from it.

Decided
Jul 2, 2021
Review
301 days
Class
Class II
Product code
MEG
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K000572 (2000). 34 ancestors in all, the oldest K822083 (1982). 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2015: 1 other ancestor2008: 1 other ancestor2004: 1 other ancestor1999: 2 other ancestors2007: 3 other ancestors2006: 1 other ancestor2003: 2 other ancestors2001: 3 other ancestors1994: 2 other ancestors2002: 2 other ancestors2000: 2 other ancestors1996: 1 other ancestor1982: 1 other ancestor1998: 1 other ancestor1997: 3 other ancestors1995: 1 other ancestor1993: 1 other ancestor2022: 1 descendant cleared2023: 1 descendant clearedK000572 · E.N.S.I. Syringe · Tri-Ject Intl. Corp. · 2000×2: 2 generations cleared close together, K020623 (2002), K022806 (2002) K031594 · Bak'snap Duopro Safety Syring (Duopross) Safety'tray Allergy Safety Syringe Tray · M.K. Meditech Co., Ltd. · 2003K050131 · Insosafe Bak'snap Retractable Insulin Safety Syringe · M.K. Meditech Co., Ltd. · 2005K152808 · U&U Insulin Syringe with/without Safety Retractable Device · U&U Medical Technology Co, Ltd. · 201619801990200020102020
  1. Root · 6 generations backK000572 E.N.S.I. SyringeTri-Ject Intl. Corp. · 2000
  2. 5 generations backK020623 Duopro Safety Syringe (Duopross)M.K. Meditech Co., Ltd. · 2002
  3. 4 generations backK022806 Duopro Safety Syringe (Duopross)M.K. Meditech Co., Ltd. · 2002
  4. 3 generations backK031594 Bak'snap Duopro Safety Syring (Duopross) Safety'tray Allergy Safety…M.K. Meditech Co., Ltd. · 2003
  5. 2 generations backK050131 Insosafe Bak'snap Retractable Insulin Safety SyringeM.K. Meditech Co., Ltd. · 2005
  6. 1 generation backK152808 U&U Insulin Syringe with/without Safety Retractable DeviceU&U Medical Technology Co, Ltd. · 2016
  7. This deviceK202570 Insulin Syringe, Insulin Syringe with Safety RetractableJiangsu Micsafe Medical Technology Co., Ltd. · 2021
  8. Descendant · cites it directly · 1 of its ownK220061 Safety Insulin SyringesBerpu Medical Technology Co., Ltd. · 2022
  9. Descendant · 2 generations on · 0 of its ownK230061 Insulin SyringeAnhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. · 2023

Most influential descendants

Showing 2 of 2 · See all
  • K220061Safety Insulin SyringesBerpu Medical Technology Co., Ltd. · 2022 · cites it directly1descendant
  • K230061Insulin SyringeAnhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. · 2023 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K000572E.N.S.I. SyringeTri-Ject Intl. Corp.2000—
−5K020623Duopro Safety Syringe (Duopross)M.K. Meditech Co., Ltd.2002—
−4K022806Duopro Safety Syringe (Duopross)M.K. Meditech Co., Ltd.2002—
−3K031594Bak'snap Duopro Safety Syring (Duopross) Safety'tray Allergy Safety Syringe TrayM.K. Meditech Co., Ltd.2003—
−2K050131Insosafe Bak'snap Retractable Insulin Safety SyringeM.K. Meditech Co., Ltd.2005—
−1K152808U&U Insulin Syringe with/without Safety Retractable DeviceU&U Medical Technology Co, Ltd.2016—
0 (this device)K202570Insulin Syringe, Insulin Syringe with Safety RetractableJiangsu Micsafe Medical Technology Co., Ltd.2021—
+1K220061Safety Insulin SyringesBerpu Medical Technology Co., Ltd.2022—
+2K230061Insulin SyringeAnhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
199310
199420
199510
199610
199730
199810
199920
200020
200130
200220
200320
200410
200610
200730
200810
201510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
202310
FIG. 1 — Lineage of K202570, 2000–2023Source: 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 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. #1 K192551 1ml Luer Slip or Luer Lock Syringe, Syringe…score 19.6 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K152808U&U Insulin Syringe with/without Safety Retractable Device
Summary page 5
…Type of Use: Prescription use only 7.3 Predicate Device Information U&U Insulin Syringe, U&U Insulin Syringe with Safety Retractable Device 510(k) Number: K152808 7.4 Device Description (1) Insulin Syringe This product uses PP, Polyisoprene rubber and SUS304 as the main materials. It co…
U&U Medical Technology Co, Ltd.2016—

Also cleared against K152808: 2 other devices →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K220061Safety Insulin SyringesBerpu Medical Technology Co., Ltd.20221

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 21 years and passes through 4 companies; a new generation was cleared every 2.2 years on median.
  • 6 of the 34 ancestors have a recall of any class.
  • Of its descendants, K220061 (Berpu Medical Technology Co., Ltd., 2022) has gone furthest, with 1 descendant of its own.
  • 2 other devices also cite its predicate K152808.

How does its category compare?

All MEG devices

MEG Syringe, Antistick: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · MEG

1in 2025

2007: 82008: 42009: 22010: 22011: 52012: 52013: 12014: 52015: 72016: 32017: 32018: 12019: 42020: 42021: 52022: 132023: 52025: 12026 (partial year): 1
2007high 13 (2022) · low 0 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MEG

229in 2023

2007: 100 days median2008: 145 days median2011: 113 days median2012: 109 days median2014: 153 days median2015: 253 days median2016: 179 days median2017: 130 days median2019: 249 days median2020: 296 days median2021: 152 days median2022: 216 days median2023: 229 days median
2007high 296 (2020) · low 100 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MEG

1in 2024

2008: 12010: 12013: 52015: 12024: 1, 1 Class I
2007high 5 (2013) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · MEG

148in 2025

2007: 212008: 202009: 262010: 342011: 342012: 222013: 272014: 362015: 512016: 942017: 1812018: 2692019: 4972020: 3532021: 5412022: 1702023: 1202024: 1122025: 148
2007high 541 (2021) · low 20 (2008)2025

MAUDE reports naming product code MEG, 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
20078100021
20084145120
20092—026
20102—134
20115113034
20125109022
20131—527
20145153036
20157253151
20163179094
201731300181
20181—0269
201942490497
202042960353
202151520541
2022132160170
202352290120
20240—1 (1)112
20251—0148
20261—0—

What is it indicated for?

The Insulin Syringe is a sterile, single use and non-reusable, insulin syringe intended for injection of U-100 insulin into the body.

The Insulin Syringe with Safety Retractable is a sterile, single use and non-reusable, manual retractable safety insulin syringe intended for injection of U-100 insulin into the body, while reducing the risk of sharps injuries and the potential for insulin syringe reuse.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K202570: Insulin Syringe, Insulin Syringe with Safety Retractable.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K202570

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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