510(k) · Cleared
ClearedStandard, Special, Special+, Sneedle B-Type and Sneedle J-Type Acupuncture Needles
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Asia-Med GmbH and CO KG · MQX Needle, Acupuncture, Single Use
Cleared on Oct 14, 2005 after a 73-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 4 later devices descend from it.
- Decided
- Oct 14, 2005
- Review
- 73 days
- Class
- Class II
- Product code
- MQX
- Recalls
- None
- Predicates
- 0
4 later devices descend from it, 2 citing it directly.
- This deviceK052085 Standard, Special, Special+, Sneedle B-Type and Sneedle J-Type…Asia-Med GmbH and CO KG · 2005
- Descendant · cites it directly · 2 of its ownK111392 Woojeon Acupuncture Needle (=Sera Acupuncture Needle)Woojeon Company · 2011
- Descendant · 2 generations on · 1 of its ownK141473 SMC Acupuncture NeedleSmc Intl., Inc. · 2014
- Descendant · 3 generations on · 0 of its ownK162566 AIK Sterile Acupuncture Needles for Single UseChangchun Aik Medical Devices Co., Ltd. · 2017
- Descendant · cites it directly · 0 of its ownK090910 Hanso Acupuncture NeedleHansol Medical Co. · 2009
Most influential descendants
Showing 4 of 4 · See all- K111392Woojeon Acupuncture Needle (=Sera Acupuncture Needle)Woojeon Company · 2011 · cites it directly2descendants
- K141473SMC Acupuncture NeedleSmc Intl., Inc. · 2014 · 2 generations on1descendant
- K162566AIK Sterile Acupuncture Needles for Single UseChangchun Aik Medical Devices Co., Ltd. · 2017 · 3 generations on0descendants
- K090910Hanso Acupuncture NeedleHansol Medical Co. · 2009 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K052085 | Standard, Special, Special+, Sneedle B-Type and Sneedle J-Type Acupuncture… | Asia-Med GmbH and CO KG | 2005 | — |
| +1 | K111392 | Woojeon Acupuncture Needle (=Sera Acupuncture Needle) | Woojeon Company | 2011 | — |
| +2 | K141473 | SMC Acupuncture Needle | Smc Intl., Inc. | 2014 | — |
| +3 | K162566 | AIK Sterile Acupuncture Needles for Single Use | Changchun Aik Medical Devices Co., Ltd. | 2017 | — |
| +1 | K090910 | Hanso Acupuncture Needle | Hansol Medical Co. | 2009 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 1 | 0 |
| 2011 | 1 | 0 |
| 2014 | 1 | 0 |
| 2017 | 1 | 0 |
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
What was it cleared against?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it? (4)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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, K111392 (Woojeon Company, 2011) has gone furthest, with 2 descendants of its own.
How does its category compare?
All MQX devicesMQX Needle, Acupuncture, Single Use: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · MQX
1in 2017
2026 to Oct 25, outlined.
Median 510(k) review, days · MQX
245in 2015
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MQX
1in 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MQX
2in 2025
MAUDE reports naming product code MQX, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 1 | — | 1 | 0 |
| 2008 | 1 | — | 0 | 2 |
| 2009 | 2 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 0 |
| 2011 | 2 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 1 | — | 0 | 1 |
| 2014 | 1 | — | 0 | 1 |
| 2015 | 3 | 245 | 0 | 1 |
| 2016 | 0 | — | 0 | 1 |
| 2017 | 1 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 1 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 1 |
| 2024 | 0 | — | 0 | 1 |
| 2025 | 0 | — | 0 | 2 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
Intended 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.
https://510kreport.com/device/K052085 · printed Nov 5, 2026
Cite this page
510(k) Report. “K052085: Standard, Special, Special+, Sneedle B-Type and Sneedle J-Type Acupuncture Needles.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K052085
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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