510(k) Report

510(k) · Cleared

Cleared

Sterile Syringe with Fixed Safety Needle for Single Use

K212652510(k) TraditionalCleared Mar 2, 2022191-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

Gemtier Medical (Shanghai), Inc. · MEG Syringe, Antistick

Cleared on Mar 2, 2022 as substantially equivalent to K192679 (Gemtier Medical (Shanghai), Inc., 2020) after a 191-day review. Its family tree reaches back 8 generations to 1977.

Decided
Mar 2, 2022
Review
191 days
Class
Class II
Product code
MEG
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K771205 (1977). 19 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 8 generations backK771205 Hypodermic SyringeTerumo America, Inc. · 1977
  2. 7 generations backK980181 Terumo Disposable Hypodermc SyringeTerumo Medical Corp. · 1998 · Recalled
  3. 6 generations backK023271 Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2002
  4. 5 generations backK052034 Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2005
  5. 4 generations backK063613 Modification to Terumo Syringe with/Without NeedleTerumo Medical Corp. · 2006
  6. 3 generations backK083514 Terumo Syringe with/Without NeedleTerumo Europe N.V. · 2009
  7. 2 generations backK170651 Sterile Disposable Syringe with Safety Needle, Sterile Disposable…Yangzhou Medline Industry, Co., Ltd. · 2017
  8. 1 generation backK192679 Sterile Syringe with Safety needle for Single Use, Sterile Syringe…Gemtier Medical (Shanghai), Inc. · 2020
  9. This deviceK212652 Sterile Syringe with Fixed Safety Needle for Single UseGemtier Medical (Shanghai), Inc. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K771205Hypodermic SyringeTerumo America, Inc.1977—
−7K980181Terumo Disposable Hypodermc SyringeTerumo Medical Corp.19981
−6K023271Terumo Syringe with/Without NeedleTerumo Medical Corp.2002—
−5K052034Terumo Syringe with/Without NeedleTerumo Medical Corp.2005—
−4K063613Modification to Terumo Syringe with/Without NeedleTerumo Medical Corp.2006—
−3K083514Terumo Syringe with/Without NeedleTerumo Europe N.V.2009—
−2K170651Sterile Disposable Syringe with Safety Needle, Sterile Disposable Syringe with…Yangzhou Medline Industry, Co., Ltd.2017—
−1K192679Sterile Syringe with Safety needle for Single Use, Sterile Syringe for Single…Gemtier Medical (Shanghai), Inc.2020—
0 (this device)K212652Sterile Syringe with Fixed Safety Needle for Single UseGemtier Medical (Shanghai), Inc.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197710
199010
199310
199810
200110
200310
200410
200510
200610
200710
201210
FIG. 1 — Lineage of K212652, 1977–2022Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
*K192679Sterile Syringe with Safety needle for Single Use, Sterile Syringe for Single Use…
Summary page 5
…1ml 25G 5/8", 1" RW 5. Identification of Predicate Device and Reference Device Predicate 510(k) Number: K192679 Predicate Product Name: Sterile Syringe with Safety needle for Single Use Reference Devices Reference Device 510(…
Gemtier Medical (Shanghai), Inc.2020—
†K210443PLPT LDV (Low Dead Volume) Sterile SyringePoonglim Pharmatech, Inc.2021—
†K210444EZ-Injec LDV Sterile Safety NeedlePoonglim Pharmatech, Inc.2021—

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 45 years and passes through 5 companies; a new generation was cleared every 2.7 years on median.
  • 4 of the 19 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. 2022, 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?

Sterile Syringe with Fixed Safety Needle for Single Use 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 mechanism can be manually activated to cover the needle immediately to minimize risk of accidental needlesticks.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K212652: Sterile Syringe with Fixed Safety Needle for Single Use.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K212652

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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