510(k) Report

510(k) · Cleared

Cleared

Seirin Acupuncture Needles

K962809510(k) TraditionalCleared Aug 16, 199629-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

Seirin-America, Inc. · MQX Needle, Acupuncture, Single Use

Cleared on Aug 16, 1996 after a 29-day review. The FDA summary names its predicate without a number. 5 later devices descend from it.

Decided
Aug 16, 1996
Review
29 days
Class
Class II
Product code
MQX
Recalls
None
Predicates
0

5 later devices descend from it, 4 citing it directly.

Descendants, by year cleared 1998: 2 descendants cleared2003: 2 descendants cleared2009: 1 descendant cleared1995200020052010201520202025
  1. This deviceK962809 Seirin Acupuncture NeedlesSeirin-America, Inc. · 1996
  2. Descendant · cites it directly · 1 of its ownK974616 Singer Acupuncture NeedlesLorac, Inc. · 1998
  3. Descendant · 2 generations on · 0 of its ownK090199 Jiajian Acupuncture NeedleWuxi Jiajian Medical Instrument Co., Ltd. · 2009
  4. Descendant · cites it directly · 0 of its ownK031060 Nano Tech and Super Nano Acupuncture NeedlesLhasa Medical, Inc. · 2003
  5. Descendant · cites it directly · 0 of its ownK023787 Tai-Chi and Master Acupuncture NeedlesLhasa Medical, Inc. · 2003
  6. Descendant · cites it directly · 0 of its ownK980899 Jin Acupuncture Needles, Models ST, GL, SI, PT, and IDKenshin Trading Corp. · 1998

Most influential descendants

Showing 5 of 5 · See all
  • K974616Singer Acupuncture NeedlesLorac, Inc. · 1998 · cites it directly1descendant
  • K090199Jiajian Acupuncture NeedleWuxi Jiajian Medical Instrument Co., Ltd. · 2009 · 2 generations on0descendants
  • K031060Nano Tech and Super Nano Acupuncture NeedlesLhasa Medical, Inc. · 2003 · cites it directly0descendants
  • K023787Tai-Chi and Master Acupuncture NeedlesLhasa Medical, Inc. · 2003 · cites it directly0descendants
  • K980899Jin Acupuncture Needles, Models ST, GL, SI, PT, and IDKenshin Trading Corp. · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K962809Seirin Acupuncture NeedlesSeirin-America, Inc.1996—
+1K974616Singer Acupuncture NeedlesLorac, Inc.1998—
+2K090199Jiajian Acupuncture NeedleWuxi Jiajian Medical Instrument Co., Ltd.2009—
+1K031060Nano Tech and Super Nano Acupuncture NeedlesLhasa Medical, Inc.2003—
+1K023787Tai-Chi and Master Acupuncture NeedlesLhasa Medical, Inc.2003—
+1K980899Jin Acupuncture Needles, Models ST, GL, SI, PT, and IDKenshin Trading Corp.1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199820
200320
200910
FIG. 1 — Lineage of K962809, 1996–2009Source: 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 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
Get a 510(k) Report

What was it cleared against? (2)

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
*—Acupuncture needles in commercial distribution prior to May 28, 1976
Named without a submission number
—
*—Other acupuncture needles currently sold through interstate commerce
Named without a submission number
—

What descends from it? (5)

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K974616Singer Acupuncture NeedlesLorac, Inc.19981
K031060Nano Tech and Super Nano Acupuncture NeedlesLhasa Medical, Inc.20030
K023787Tai-Chi and Master Acupuncture NeedlesLhasa Medical, Inc.20030
K980899Jin Acupuncture Needles, Models ST, GL, SI, PT, and IDKenshin Trading Corp.19980

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, K974616 (Lorac, Inc., 1998) has gone furthest, with 1 descendant 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?

Acupuncture needles are defined as devices intended to pierce the skin in the practice of acupuncture by qualified practitioners of acupuncture as determined by the States.

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. “K962809: Seirin 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/K962809

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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