510(k) Report

510(k) · Cleared

Cleared

Needle Stimulator

K202861510(k) TraditionalCleared Aug 27, 2021333-day reviewClass U

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

Wuxi Jiajian Medical Instrument Co., Ltd. · BWK Stimulator, Electro-Acupuncture

Cleared on Aug 27, 2021 as substantially equivalent to K130768 (Wuxi Jiajian Medical Instrument Co., Ltd., 2013) after a 333-day review. Its family tree reaches back 5 generations to 1996. 2 later devices descend from it.

Decided
Aug 27, 2021
Review
333 days
Class
Class U
Product code
BWK
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K954334 (1996). 6 ancestors in all, the oldest K840983 (1984). 2 later devices descend from it, 2 citing it directly.

  1. Root · 5 generations backK954334 AcuplusS.H.P. Intl. Pty., Ltd. · 1996
  2. 4 generations backK014273 AcustimS.H.P. Intl. Pty., Ltd. · 2002
  3. 3 generations backK051197 Aculife, Model SMW-01Inno-Health Technology, Inc. · 2006
  4. 2 generations backK081943 Model ES-130Ito Co., Ltd. · 2008
  5. 1 generation backK130768 Jiajian CMN StimulatorWuxi Jiajian Medical Instrument Co., Ltd. · 2013
  6. This deviceK202861 Needle StimulatorWuxi Jiajian Medical Instrument Co., Ltd. · 2021
  7. Descendant · cites it directly · 0 of its ownK244030 Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)Wuxi Jiajian Medical Instrument Co., Ltd. · 2025
  8. Descendant · cites it directly · 0 of its ownK220153 Needle Stimulator (Model: RJNS6-1)Bozhou Rongjian Medical Appliance Co., Ltd. · 2022

Most influential descendants

Showing 2 of 2 · See all
  • K244030Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)Wuxi Jiajian Medical Instrument Co., Ltd. · 2025 · cites it directly0descendants
  • K220153Needle Stimulator (Model: RJNS6-1)Bozhou Rongjian Medical Appliance Co., Ltd. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K954334AcuplusS.H.P. Intl. Pty., Ltd.1996—
−4K014273AcustimS.H.P. Intl. Pty., Ltd.2002—
−3K051197Aculife, Model SMW-01Inno-Health Technology, Inc.2006—
−2K081943Model ES-130Ito Co., Ltd.2008—
−1K130768Jiajian CMN StimulatorWuxi Jiajian Medical Instrument Co., Ltd.2013—
0 (this device)K202861Needle StimulatorWuxi Jiajian Medical Instrument Co., Ltd.2021—
+1K244030Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)Wuxi Jiajian Medical Instrument Co., Ltd.2025—
+1K220153Needle Stimulator (Model: RJNS6-1)Bozhou Rongjian Medical Appliance Co., Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
202510
FIG. 1 — Lineage of K202861, 1996–2025Source: 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 BWK? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new BWK device

  1. #1 K244030 Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)score 10.6 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

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
*K130768Jiajian CMN Stimulator
Summary page 4
…eters Modified Device Predicate Device Remark 1 510(k) Number: K202861 K130768 -- Marketing clearance…
Wuxi Jiajian Medical Instrument Co., Ltd.2013—

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K244030Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)Wuxi Jiajian Medical Instrument Co., Ltd.20250
K220153Needle Stimulator (Model: RJNS6-1)Bozhou Rongjian Medical Appliance Co., Ltd.20220

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?

  • The line of descent spans 25 years and passes through 4 companies; a new generation was cleared every 4.7 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K244030 (Wuxi Jiajian Medical Instrument Co., Ltd., 2025) has gone furthest, with 0 descendants of its own.

How does its category compare?

All BWK devices

BWK Stimulator, Electro-Acupuncture: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · BWK

1in 2025

2008: 12009: 12010: 22013: 22014: 32015: 12016: 12017: 12021: 22022: 12025: 12026 (partial year): 1
2007high 3 (2014) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BWK

212in 2014

2014: 212 days median
2007high 212 (2014)2026

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

Recalls per year · BWK

No recall names BWK since 2007.

Adverse event reports per year · BWK

1in 2024

2012: 12018: 12023: 12024: 1
2007high 1 (2012) · low 0 (2007)2025

MAUDE reports naming product code BWK, 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
20070—00
20081—00
20091—00
20102—00
20110—00
20120—01
20132—00
2014321200
20151—00
20161—00
20171—00
20180—01
20190—00
20200—00
20212—00
20221—00
20230—01
20240—01
20251—00
20261—0—

What is it indicated for?

Needle Stimulator is an electro-acupuncture stimulator device, which is indicated for use 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. “K202861: Needle Stimulator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K202861

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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