510(k) Report

510(k) · Cleared

Cleared

NeuroTrigger Basic (NTB)

K223027510(k) TraditionalCleared Oct 10, 2023376-day reviewClass II21 CFR 890.5850

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

Neurotrigger · IPF Stimulator, Muscle, Powered

Cleared on Oct 10, 2023 as substantially equivalent to K193275 (Shenzhen Xft Medical Limited, 2020) after a 376-day review. Its family tree reaches back 7 generations to 1991.

Decided
Oct 10, 2023
Review
376 days
Class
Class II
Product code
IPF
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K912178 (1991). 19 ancestors in all, the oldest K880042 (1988). No later device cites it as a predicate yet.

  1. Root · 7 generations backK912178 Bio Tens 601, 606 and 608 (3000)Skylark Device Co., Ltd. · 1991
  2. 6 generations backK972244 NT2000Bio-Medical Research, Ltd. · 1998
  3. 5 generations backK990787 TRIO 300Ito Co., Ltd. · 1999
  4. 4 generations backK023231 Elfcare Device, Models 314A Through 314GMediseb, Ltd. · 2003
  5. 3 generations backK070299 Ezfit Digital Heating Tens (Model NO.: HR-661/UC-101)Ezfit Technology, Inc. · 2007
  6. 2 generations backK162517 Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13Jkh Health Co., Ltd. · 2017
  7. 1 generation backK193275 Nerve and Muscle StimulatorShenzhen Xft Medical Limited · 2020
  8. This deviceK223027 NeuroTrigger Basic (NTB)Neurotrigger · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K912178Bio Tens 601, 606 and 608 (3000)Skylark Device Co., Ltd.1991—
−6K972244NT2000Bio-Medical Research, Ltd.1998—
−5K990787TRIO 300Ito Co., Ltd.1999—
−4K023231Elfcare Device, Models 314A Through 314GMediseb, Ltd.2003—
−3K070299Ezfit Digital Heating Tens (Model NO.: HR-661/UC-101)Ezfit Technology, Inc.2007—
−2K162517Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13Jkh Health Co., Ltd.2017—
−1K193275Nerve and Muscle StimulatorShenzhen Xft Medical Limited2020—
0 (this device)K223027NeuroTrigger Basic (NTB)Neurotrigger2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199110
199410
199510
199710
199810
199910
200220
200510
200810
201610
FIG. 1 — Lineage of K223027, 1991–2023Source: 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 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. #1 K241433 EVE Synergy (EVE-20M)score 19.7 · 25 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
*K193275Nerve and Muscle Stimulator
Summary page 6
…Stimulator Product Code: IPF Device Class: II Review Panel: Physical Medicine Regulation Number: 21 CFR 890.5850 Predicate Device: Shenzhen XFT-2000 (K193275) Device Description: The NeuroTrigger Basic (NTB) powered muscle stimulator is composed of a hardware component encased in Ac…
Shenzhen Xft Medical Limited2020—
†K220994Shoulder PacemakerTMNcs Lab Srl2022—
†K071137Sonicator Plus 940, Model ME940Mettler Electronics Corp.2007—
†K153224VitalStim (R) Plus Electrotherapy SystemDjo, LLC2016—
†K210938PowerDot PD-01MT2 Muscle StimulatorSmartmissimo Technologies Pte, Ltd.2021—

Also cleared against K193275: 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?

  • The line of descent spans 32 years and passes through 8 companies; a new generation was cleared every 3.5 years on median.
  • None of the 19 ancestors has a recall.
  • 1 other device also cites its predicate K193275.

How does its category compare?

All IPF devices

IPF Stimulator, Muscle, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · IPF

3in 2025

2007: 82008: 62009: 72010: 42011: 42012: 42013: 102014: 42015: 32016: 72017: 52018: 52019: 42020: 92021: 152022: 72023: 92024: 72025: 32026 (partial year): 3
2007high 15 (2021) · low 3 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IPF

257in 2025

2007: 143 days median2008: 140 days median2009: 216 days median2010: 121 days median2011: 275 days median2012: 269 days median2013: 180 days median2014: 264 days median2015: 43 days median2016: 113 days median2017: 110 days median2018: 73 days median2019: 133 days median2020: 121 days median2021: 98 days median2022: 108 days median2023: 255 days median2024: 201 days median2025: 257 days median2026 (partial year): 206 days median
2007high 275 (2011) · low 43 (2015)2026

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

Recalls per year · IPF

1in 2023

2008: 12011: 12012: 32023: 1
2007high 3 (2012) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · IPF

8in 2025

2007: 112008: 2132009: 1502010: 142011: 252012: 162013: 62014: 192015: 112016: 82017: 22018: 32019: 102020: 132021: 32022: 42023: 82024: 52025: 8
2007high 213 (2008) · low 2 (2017)2025

MAUDE reports naming product code IPF, 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
20078143011
200861401213
200972160150
20104121014
20114275125
20124269316
20131018006
20144264019
2015343011
2016711308
2017511002
201857303
20194133010
20209121013
2021159803
2022710804
2023925518
2024720105
2025325708
202632060—

What is it indicated for?

NeuroTrigger Basic is indicated for the prevention or retardation of disuse atrophy, muscle re-education, and for maintaining or increasing range of motion.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K223027: NeuroTrigger Basic (NTB).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K223027

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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