510(k) Report

510(k) · Cleared

Cleared

Hypodermic Safety Needle; Hypodermic Safety Needle with Syringe

K211555510(k) TraditionalCleared Oct 18, 2021152-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

Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. · MEG Syringe, Antistick

Cleared on Oct 18, 2021 as substantially equivalent to K190183 (Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd., 2019) after a 152-day review. Its family tree reaches back 7 generations to 1990.

Decided
Oct 18, 2021
Review
152 days
Class
Class II
Product code
MEG
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K904198 (1990). 12 ancestors in all, the oldest K771205 (1977). No later device cites it as a predicate yet.

  1. Root · 7 generations backK904198 Safety Needle SheathConcord/Portex · 1990
  2. 6 generations backK923127 Needle-Pro CartridgeConcord/Portex · 1993 · Recalled
  3. 5 generations backK031453 Terumo Surguard 2 Safety NeedleTerumo Medical Corp. · 2003
  4. 4 generations backK040531 Terumo SURGUARD2 Safety NeedleTerumo Medical Corp. · 2004
  5. 3 generations backK051865 Terumo Surguard 2 Safety Needle or SimilarTerumo Medical Corp. · 2005
  6. 2 generations backK113422 Terumo Surguard 3 Safety Needle Terumo Surguard 3 Hypodermic Syringe…Terumo (Philippines) Corporation · 2012
  7. 1 generation backK190183 Hypodermic Safety Needle, Hypodermic Safety Needle with SyringeAnhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. · 2019
  8. This deviceK211555 Hypodermic Safety Needle; Hypodermic Safety Needle with SyringeAnhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. · 2021
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K904198Safety Needle SheathConcord/Portex1990—
−6K923127Needle-Pro CartridgeConcord/Portex19931
−5K031453Terumo Surguard 2 Safety NeedleTerumo Medical Corp.2003—
−4K040531Terumo SURGUARD2 Safety NeedleTerumo Medical Corp.2004—
−3K051865Terumo Surguard 2 Safety Needle or SimilarTerumo Medical Corp.2005—
−2K113422Terumo Surguard 3 Safety Needle Terumo Surguard 3 Hypodermic Syringe with…Terumo (Philippines) Corporation2012—
−1K190183Hypodermic Safety Needle, Hypodermic Safety Needle with SyringeAnhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.2019—
0 (this device)K211555Hypodermic Safety Needle; Hypodermic Safety Needle with SyringeAnhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197720
199810
200110
200210
FIG. 1 — Lineage of K211555, 1990–2021Source: 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
*K190183Hypodermic Safety Needle, Hypodermic Safety Needle with Syringe
Summary page 4
…MEG FMI FMF Device Class: Class II Predicate Device: K190183 Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. === Pag…
Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.2019—
†K060211Wuzhou Syringe, with/Without NeedleWenzhou Wuzhou Group Co., Ltd.2006—

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 31 years and passes through 4 companies; a new generation was cleared every 2.4 years on median.
  • 3 of the 12 ancestors have a recall of any class.

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?

Hypodermic Safety Needle with Syringe The Hypodermic Safety Needle with Syringe is intended for use in the aspiration and injection of fluids for medical purpose. After withdrawal of the needle from the body, the attached needle safety shield can be manually activated to cover the needle immediately after use to minimize risk of accidental needle sticks. Hypodermic Safety Needle The Hypodermic Safety Needle is intended to be used with a luer lock syringe…

Read the full statement (112 words)

Hypodermic Safety Needle with Syringe

The Hypodermic Safety Needle with Syringe is intended for use in the aspiration and injection of fluids for medical purpose. After withdrawal of the needle from the body, the attached needle safety shield can be manually activated to cover the needle immediately after use to minimize risk of accidental needle sticks.

Hypodermic Safety Needle

The Hypodermic Safety Needle is intended to be used with a luer lock syringe for aspiration and injection of fluids for medical purpose. After withdrawal of the needle from the body, the attached needle safety shield can be manually activated to cover the needle immediately after use to minimize risk of accidental needlestick.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K211555: Hypodermic Safety Needle; Hypodermic Safety Needle with Syringe.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K211555

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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