510(k) Report

510(k) · Cleared

Cleared

Tai-Chi and Master Acupuncture Needles

K023787510(k) SpecialCleared Feb 14, 200393-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

Lhasa Medical, Inc. · MQX Needle, Acupuncture, Single Use

Cleared on Feb 14, 2003 as substantially equivalent to K003760 (Lhasa Medical, Inc., 2001) and 1 other predicate after a 93-day review. Its family tree reaches back 1 generation to 1996.

Decided
Feb 14, 2003
Review
93 days
Class
Class II
Product code
MQX
Recalls
None
Predicates
2

Its longest line of descent runs back 1 generation to K962809 (1996). 2 ancestors in all. No later device cites it as a predicate yet.

Other ancestors, by year cleared 2001: 1 other ancestorK962809 · Seirin Acupuncture Needles · Seirin-America, Inc. · 199619961998200020022004
Other ancestors, by generation 1 generation back: 1 other ancestor K962809 · Seirin Acupuncture Needles · Seirin-America, Inc. · 19960
  1. Root · 1 generation backK962809 Seirin Acupuncture NeedlesSeirin-America, Inc. · 1996
  2. This deviceK023787 Tai-Chi and Master Acupuncture NeedlesLhasa Medical, Inc. · 2003
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K962809Seirin Acupuncture NeedlesSeirin-America, Inc.1996—
0 (this device)K023787Tai-Chi and Master Acupuncture NeedlesLhasa Medical, Inc.2003—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110
FIG. 1 — Lineage of K023787, 1996–2003Source: 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.

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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? (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
*K003760Tai-Chi Acupuncture Needles
Summary page 1
…ure needles which have received approval through the 5 10(k) premarket notification process. These include the following: Tai-Chi Acupuncture Needles K-003760 (2/6/01) SEIRIN Acupuncture Needles K-962809 (8/16/92) ....... continued on next page…
Lhasa Medical, Inc.2001—
*K962809Seirin Acupuncture Needles
Summary page 1
…k) premarket notification process. These include the following: Tai-Chi Acupuncture Needles K-003760 (2/6/01) SEIRIN Acupuncture Needles K-962809 (8/16/92) ....... continued on next page LHASA MEDICAL, INC.…
Seirin-America, Inc.1996—

Also cleared against K003760: 1 other device →

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?

  • None of the 2 ancestors has a recall.
  • 1 other device also cites its predicate K003760.

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?

These acupuncture needles are used 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 summary.

Cite this page

510(k) Report. “K023787: Tai-Chi and Master 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/K023787

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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