510(k) · Cleared
ClearedTENS & EMS DEVICE (Model: FM-B2403A)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Shenzhen Jian Feng Electronic Technology Co., Ltd. · NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
Cleared on Mar 8, 2022 as substantially equivalent to K202866 (Shenzhen Jian Feng Electronic Technology Co., Ltd., 2021) after a 99-day review. Its family tree reaches back 8 generations to 1994. 1 later device descends from it.
- Decided
- Mar 8, 2022
- Review
- 99 days
- Class
- Class II
- Product code
- NUH
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 8 generations to K940301 (1994). 11 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 8 generations backK940301 Compex 2Biodex Medical Systems, Inc. · 1994
- 7 generations backK011880 Compex SportCompex S.A. · 2002
- 6 generations backK060846 Therapeutic Massage CompanionEndurance Therapeutics · 2007
- 5 generations backK110068 Model PM3030Omron Healthcare, Inc. · 2011
- 4 generations backK132993 Counter Otc Tens DeviceCounter Scientific Development (Gz), Ltd. · 2014
- 3 generations backK150386 Tyece OTC TENS DeviceTyece, Ltd. · 2015
- 2 generations backK171803 HIVOX OTC Electrical StimulatorHivox Biotek, Inc. · 2017
- 1 generation backK202866 TENS & EMS DeviceShenzhen Jian Feng Electronic Technology Co., Ltd. · 2021
- This deviceK213741 TENS & EMS DEVICE (Model: FM-B2403A)Shenzhen Jian Feng Electronic Technology Co., Ltd. · 2022
- Descendant · cites it directly · 0 of its ownK243131 Triathlon ProSigma Biomedical · 2025
Most influential descendants
Showing 1 of 1 · See all- K243131Triathlon ProSigma Biomedical · 2025 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −8 | K940301 | Compex 2 | Biodex Medical Systems, Inc. | 1994 | — |
| −7 | K011880 | Compex Sport | Compex S.A. | 2002 | — |
| −6 | K060846 | Therapeutic Massage Companion | Endurance Therapeutics | 2007 | — |
| −5 | K110068 | Model PM3030 | Omron Healthcare, Inc. | 2011 | — |
| −4 | K132993 | Counter Otc Tens Device | Counter Scientific Development (Gz), Ltd. | 2014 | — |
| −3 | K150386 | Tyece OTC TENS Device | Tyece, Ltd. | 2015 | — |
| −2 | K171803 | HIVOX OTC Electrical Stimulator | Hivox Biotek, Inc. | 2017 | — |
| −1 | K202866 | TENS & EMS Device | Shenzhen Jian Feng Electronic Technology Co., Ltd. | 2021 | — |
| 0 (this device) | K213741 | TENS & EMS DEVICE (Model: FM-B2403A) | Shenzhen Jian Feng Electronic Technology Co., Ltd. | 2022 | — |
| +1 | K243131 | Triathlon Pro | Sigma Biomedical | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2004 | 1 | 0 |
| 2005 | 1 | 0 |
| 2013 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2025 | 1 | 0 |
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 NUH? 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 NUH device
- #1 K190783 Health Expert Electronic Stimulator (model…score 15.8 · 7 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K202866 | TENS & EMS DeviceSummary page 5…ail：[email protected] Device Name TENS & EMS Device Model FM-B2403 510(K) Number K202866 Product Code NUH, NGX Panel Code Physical Medicine, Neurology… | 2021 |
| † | K092546 | Gmdasz Tens Electrodes, Models CWN1005, Dia. 5CM, DWN2505, 5CMX5CM, CWN1007.Dia. 7CM… | 2009 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K243131 | Triathlon Pro | 2025 | 0 |
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 28 years and passes through 8 companies; a new generation was cleared every 3.5 years on median.
- None of the 11 ancestors has a recall.
- Of its descendants, K243131 (Sigma Biomedical, 2025) has gone furthest, with 0 descendants of its own.
- 1 other device also cites its predicate K202866.
How does its category compare?
All NUH devicesNUH Stimulator, Nerve, Transcutaneous, Over-The-Counter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.
FDA decisions per year · NUH
15in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NUH
119in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NUH
No recall names NUH since 2007.
Adverse event reports per year · NUH
7in 2025
MAUDE reports naming product code NUH, 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 | 4 | 161 | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 3 | 148 | 0 | 0 |
| 2011 | 6 | 231 | 0 | 0 |
| 2012 | 6 | 170 | 0 | 0 |
| 2013 | 10 | 189 | 0 | 1 |
| 2014 | 16 | 212 | 0 | 9 |
| 2015 | 14 | 198 | 0 | 11 |
| 2016 | 13 | 145 | 0 | 13 |
| 2017 | 17 | 155 | 0 | 21 |
| 2018 | 16 | 121 | 0 | 18 |
| 2019 | 19 | 213 | 0 | 5 |
| 2020 | 14 | 147 | 0 | 8 |
| 2021 | 14 | 198 | 0 | 7 |
| 2022 | 20 | 103 | 0 | 2 |
| 2023 | 15 | 127 | 0 | 4 |
| 2024 | 20 | 90 | 0 | 7 |
| 2025 | 15 | 119 | 0 | 7 |
| 2026 | 5 | 137 | 0 | — |
What is it indicated for?
TENS:
The device is designed to be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back, neck, upper extremities (arm), lower extremities (leg), abdomen and bottom due to strain from exercise or normal household work activities.
EMS:
The device is designed to be used to stimulate healthy muscles in order to improve or facilitate muscle performance.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K213741 · printed Nov 6, 2026
Cite this page
510(k) Report. “K213741: TENS & EMS DEVICE (Model: FM-B2403A).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K213741
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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