510(k) · Cleared
ClearedNerve and Muscle Stimulator
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Shenzhen Xft Medical Limited · IPF Stimulator, Muscle, Powered
Cleared on Jul 8, 2021 as substantially equivalent to K053266 (Thought Technology, Ltd., 2005) after an 87-day review. Its family tree reaches back 3 generations to 1988.
- Decided
- Jul 8, 2021
- Review
- 87 days
- Class
- Class II
- Product code
- IPF
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K880235 (1988). 4 ancestors in all. No later device cites it as a predicate yet.
- Root · 3 generations backK880235 Intelect Model 120Chattanooga Group, Inc. · 1988
- 2 generations backK031017 Sys*Stim 208 and 208AMettler Electronics Corp. · 2003
- 1 generation backK053266 Myotrac InfinitiThought Technology, Ltd. · 2005
- This deviceK211094 Nerve and Muscle StimulatorShenzhen Xft Medical Limited · 2021
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K880235 | Intelect Model 120 | Chattanooga Group, Inc. | 1988 | — |
| −2 | K031017 | Sys*Stim 208 and 208A | Mettler Electronics Corp. | 2003 | — |
| −1 | K053266 | Myotrac Infiniti | Thought Technology, Ltd. | 2005 | — |
| 0 (this device) | K211094 | Nerve and Muscle Stimulator | Shenzhen Xft Medical Limited | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 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 IPF? 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 IPF device
- #1 K241433 EVE Synergy (EVE-20M)score 19.6 · 25 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 |
|---|---|---|---|
| * | K053266 | Myotrac InfinitiSummary page 5…logy Ltd. Device: Powered muscle stimulator and biofeedback device Device#: SA9800 Trade name: MYOTRAC INFINITI 510(K) Number: K053266 4 Device Description The Nerve and Muscle Stimulator (model: XFT-2003K) is an electrical muscle stimulator for contraction of… | 2005 |
| † | K172933 | Unnamed device | |
| † | K182203 | JKH Stimulator Plus | 2019 |
| † | K191151 | JKH Stimulator Plus | 2019 |
| † | K162517 | Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13 | 2017 |
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?
- The line of descent spans 33 years and passes through 4 companies; a new generation was cleared every 15.1 years on median.
- None of the 4 ancestors has a recall.
- 1 other device also cites its predicate K053266.
How does its category compare?
All IPF devicesIPF Stimulator, Muscle, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.
FDA decisions per year · IPF
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · IPF
257in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IPF
1in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IPF
8in 2025
MAUDE reports naming product code IPF, 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 | 8 | 143 | 0 | 11 |
| 2008 | 6 | 140 | 1 | 213 |
| 2009 | 7 | 216 | 0 | 150 |
| 2010 | 4 | 121 | 0 | 14 |
| 2011 | 4 | 275 | 1 | 25 |
| 2012 | 4 | 269 | 3 | 16 |
| 2013 | 10 | 180 | 0 | 6 |
| 2014 | 4 | 264 | 0 | 19 |
| 2015 | 3 | 43 | 0 | 11 |
| 2016 | 7 | 113 | 0 | 8 |
| 2017 | 5 | 110 | 0 | 2 |
| 2018 | 5 | 73 | 0 | 3 |
| 2019 | 4 | 133 | 0 | 10 |
| 2020 | 9 | 121 | 0 | 13 |
| 2021 | 15 | 98 | 0 | 3 |
| 2022 | 7 | 108 | 0 | 4 |
| 2023 | 9 | 255 | 1 | 8 |
| 2024 | 7 | 201 | 0 | 5 |
| 2025 | 3 | 257 | 0 | 8 |
| 2026 | 3 | 206 | 0 | — |
What is it indicated for?
sEMG:
Biofeedback, Relaxation & Muscle Re-Education purposes;
NMES (muscle stimulation) and SEMG triggered stimulation (IncludingETS, PAS and MIRROR Mode):
1) Relaxation of muscle spasms;
2) Prevention or retardation of disuse atrophy;
3) Increasing local blood circulation;
4) Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis;
5) Maintaining or increasing range of motion;
6) Stroke Rehab by Muscle re-education.
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/K211094 · printed Nov 6, 2026
Cite this page
510(k) Report. “K211094: Nerve and Muscle Stimulator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K211094
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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