510(k) Report

510(k) · Cleared

Cleared

Shenling Acupuncture Needles

K002411510(k) TraditionalCleared Dec 12, 2000127-day reviewClass II21 CFR 880.5580

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Shenling Medical Device Co., Ltd. · MQX Needle, Acupuncture, Single Use

Cleared on Dec 12, 2000 after a 127-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 1 later device descends from it.

Decided
Dec 12, 2000
Review
127 days
Class
Class II
Product code
MQX
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2002: 1 descendant cleared200020052010201520202025
  1. This deviceK002411 Shenling Acupuncture NeedlesShenling Medical Device Co., Ltd. · 2000
  2. Descendant · cites it directly · 0 of its ownK023054 Jia Chen Acupuncture Needle, for Single UseMandala Health Care, LLC · 2002

Most influential descendants

Showing 1 of 1 · See all
  • K023054Jia Chen Acupuncture Needle, for Single UseMandala Health Care, LLC · 2002 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K002411Shenling Acupuncture NeedlesShenling Medical Device Co., Ltd.2000—
+1K023054Jia Chen Acupuncture Needle, for Single UseMandala Health Care, LLC2002—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
FIG. 1 — Lineage of K002411, 2000–2002Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K023054Jia Chen Acupuncture Needle, for Single UseMandala Health Care, LLC20020

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?

  • Of its descendants, K023054 (Mandala Health Care, LLC, 2002) has gone furthest, with 0 descendants of its own.

How does its category compare?

All MQX devices

MQX Needle, Acupuncture, Single Use: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MQX

1in 2017

2007: 12008: 12009: 22010: 12011: 22013: 12014: 12015: 32017: 1
2007high 3 (2015) · low 0 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQX

245in 2015

2015: 245 days median
2007high 245 (2015)2026

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

Recalls per year · MQX

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MQX

2in 2025

2008: 22013: 12014: 12015: 12016: 12018: 12023: 12024: 12025: 2
2007high 2 (2008) · low 0 (2007)2025

MAUDE reports naming product code MQX, 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
20071—10
20081—02
20092—00
20101—00
20112—00
20120—00
20131—01
20141—01
2015324501
20160—01
20171—00
20180—01
20190—00
20200—00
20210—00
20220—00
20230—01
20240—01
20250—02
20260—0—
Cite this page

510(k) Report. “K002411: Shenling Acupuncture Needles.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K002411

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026