510(k) · Cleared
ClearedAB Command Dual Channel Fitness Belt
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Leto Enterprises Incorporation · NGX Stimulator, Muscle, Powered, For Muscle Conditioning
Cleared on Dec 21, 2012 as substantially equivalent to K102295 (Leto Enterprises Incorporation, 2011) after a 135-day review. Its family tree reaches back 5 generations to 2001.
- Decided
- Dec 21, 2012
- Review
- 135 days
- Class
- Class II
- Product code
- NGX
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 5 generations to K010335 (2001). No later device cites it as a predicate yet.
- Root · 5 generations backK010335 Slendertone Flex, Model, 512Bio-Medical Research, Ltd. · 2001
- 4 generations backK030708 Slendertone Flex Abdominal Training System, Type 515Bio-Medical Research, Ltd. · 2003
- 3 generations backK061914 Sport-Elec, Models Duo CT5 Slimness and CT5 SlimnessSport-Elec S.A. · 2007
- 2 generations backK081026 Body Control System Family, Body Control Duo and CT5Sport-Elec S.A. · 2008
- 1 generation backK102295 X2ABS Dual Channel Fitness BeltLeto Enterprises Incorporation · 2011
- This deviceK122414 AB Command Dual Channel Fitness BeltLeto Enterprises Incorporation · 2012
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K010335 | Slendertone Flex, Model, 512 | Bio-Medical Research, Ltd. | 2001 | — |
| −4 | K030708 | Slendertone Flex Abdominal Training System, Type 515 | Bio-Medical Research, Ltd. | 2003 | — |
| −3 | K061914 | Sport-Elec, Models Duo CT5 Slimness and CT5 Slimness | Sport-Elec S.A. | 2007 | — |
| −2 | K081026 | Body Control System Family, Body Control Duo and CT5 | Sport-Elec S.A. | 2008 | — |
| −1 | K102295 | X2ABS Dual Channel Fitness Belt | Leto Enterprises Incorporation | 2011 | — |
| 0 (this device) | K122414 | AB Command Dual Channel Fitness Belt | Leto Enterprises Incorporation | 2012 | — |
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 NGX? 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 NGX device
- #1 K250146 SofWave Systemscore 15.5 · 12 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 |
|---|---|---|---|
| * | K102295 | X2ABS Dual Channel Fitness BeltSummary page 1…Device Information Submitter: Leto Enterprises Incorporation Device Name: X2ABS Dual Channel Fitness Belt 5 10(K) Number: K102295 Report by MEDLAB (Shenzheri) Information Service Co., Ltd. Page 9-1 Sponsor:, L… | 2011 |
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 11 years and passes through 3 companies; a new generation was cleared every 1.8 years on median.
- None of the 5 ancestors has a recall.
- 3 other devices also cite its predicate K102295.
How does its category compare?
All NGX devicesNGX Stimulator, Muscle, Powered, For Muscle Conditioning: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.
FDA decisions per year · NGX
15in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NGX
93in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NGX
2in 2013
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NGX
15in 2025
MAUDE reports naming product code NGX, 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 | 7 | 135 | 0 | 0 |
| 2008 | 3 | 209 | 0 | 0 |
| 2009 | 4 | 132 | 0 | 0 |
| 2010 | 6 | 180 | 0 | 0 |
| 2011 | 5 | 291 | 0 | 1 |
| 2012 | 3 | 362 | 0 | 0 |
| 2013 | 6 | 269 | 2 | 1 |
| 2014 | 6 | 298 | 0 | 0 |
| 2015 | 9 | 184 | 0 | 7 |
| 2016 | 4 | 240 | 0 | 21 |
| 2017 | 10 | 108 | 0 | 2 |
| 2018 | 6 | 104 | 0 | 6 |
| 2019 | 14 | 167 | 0 | 4 |
| 2020 | 11 | 207 | 0 | 7 |
| 2021 | 12 | 256 | 0 | 5 |
| 2022 | 6 | 307 | 0 | 7 |
| 2023 | 12 | 96 | 0 | 8 |
| 2024 | 12 | 207 | 0 | 11 |
| 2025 | 15 | 93 | 0 | 15 |
| 2026 | 4 | 118 | 0 | — |
What is it indicated for?
The AB COMMAND Dual Channel Fitness Belt is indicated for the improvement of
muscle tone, for strengthening of muscles and for the development of firmer muscles. It
is indicated for use on the abdominal muscles.
Contraindicated use on injured or otherwise impaired muscles.
Not intended for use in any therapy or for the treatment of any medical conditions or
diseases.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K122414 · printed Nov 6, 2026
Cite this page
510(k) Report. “K122414: AB Command Dual Channel Fitness Belt.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K122414
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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