510(k) Report

510(k) · Cleared

Cleared

C&G Acupuncture Needle

K043277510(k) TraditionalCleared Feb 8, 200574-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

Helio Medical Supplies, Inc. · MQX Needle, Acupuncture, Single Use

Cleared on Feb 8, 2005 after a 74-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 1 later device descends from it.

Decided
Feb 8, 2005
Review
74 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 2010: 1 descendant cleared20052010201520202025
  1. This deviceK043277 C&G Acupuncture NeedleHelio Medical Supplies, Inc. · 2005
  2. Descendant · cites it directly · 0 of its ownK092240 Acupuncture NeedlesHaenglim Seowon Medical Co. · 2010

Most influential descendants

Showing 1 of 1 · See all
  • K092240Acupuncture NeedlesHaenglim Seowon Medical Co. · 2010 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K043277C&G Acupuncture NeedleHelio Medical Supplies, Inc.2005—
+1K092240Acupuncture NeedlesHaenglim Seowon Medical Co.2010—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
FIG. 1 — Lineage of K043277, 2005–2010Source: 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 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in MQX? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • 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’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K092240Acupuncture NeedlesHaenglim Seowon Medical Co.20100

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, K092240 (Haenglim Seowon Medical Co., 2010) 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—

What is it indicated for?

To pierce the skin in the practice of acupuncture by qualified practitioners of acupuncture as determined by the States.

Indications for use as stated in the FDA 510(k) statement.

Cite this page

510(k) Report. “K043277: C&G Acupuncture Needle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K043277

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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