510(k) Report

510(k) · Cleared

Cleared

Intonemv

K134020510(k) TraditionalCleared Feb 25, 201457-day reviewClass II21 CFR 876.5320

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

Incontrol Medical, LLC · KPI Stimulator, Electrical, Non-Implantable, For Incontinence

Cleared on Feb 25, 2014 as substantially equivalent to K110179 (Incontrol Medical, LLC, 2012) and 1 other predicate after a 57-day review. Its family tree reaches back 8 generations to 1995. 10 later devices descend from it.

Decided
Feb 25, 2014
Review
57 days
Class
Class II
Product code
KPI
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K930530 (1995). 25 ancestors in all, the oldest K813008 (1981). 10 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2003: 3 other ancestors2000: 2 other ancestors2004: 2 other ancestors2001: 3 other ancestors1997: 1 other ancestor1994: 1 other ancestor1998: 1 other ancestor1996: 1 other ancestor1987: 1 other ancestor1986: 1 other ancestor1981: 1 other ancestor2019: 1 descendant cleared2015: 1 descendant cleared2018: 1 descendant cleared2023: 2 descendants cleared2026: 3 descendants cleared2025: 2 descendants clearedK930530 · Incare PRS 9300 Pelvic FL Thera Syst/Treat Uri Inc · Hollister, Inc. · 1995K961872 · Incare Pelvic Floor Therapy System with Desktop Computer · Hollister, Inc. · 1996K974048 · Incare Pelvic Floor Therapy System with Desktop Computer · Hollister, Inc. · 1997K013612 · Incare Pelvic Floor Therapy System · Hollister, Inc. · 2002K050483 · Evadri Bladder Control Systems · Hollister, Inc. · 2005K053434 · Myotrac Infiniti Electrical Stimulator · Thought Technology, Ltd. · 2006K080950 · Stiwell MED4 · Otto Bock, Austria GmbH · 2009K110179 · Incontrol · Incontrol Medical, LLC · 201219801990200020102020
  1. Root · 8 generations backK930530 Incare PRS 9300 Pelvic FL Thera Syst/Treat Uri IncHollister, Inc. · 1995
  2. 7 generations backK961872 Incare Pelvic Floor Therapy System with Desktop ComputerHollister, Inc. · 1996
  3. 6 generations backK974048 Incare Pelvic Floor Therapy System with Desktop ComputerHollister, Inc. · 1997
  4. 5 generations backK013612 Incare Pelvic Floor Therapy SystemHollister, Inc. · 2002
  5. 4 generations backK050483 Evadri Bladder Control SystemsHollister, Inc. · 2005
  6. 3 generations backK053434 Myotrac Infiniti Electrical StimulatorThought Technology, Ltd. · 2006
  7. 2 generations backK080950 Stiwell MED4Otto Bock, Austria GmbH · 2009
  8. 1 generation backK110179 IncontrolIncontrol Medical, LLC · 2012
  9. This deviceK134020 IntonemvIncontrol Medical, LLC · 2014
  10. Descendant · cites it directly · 6 of its ownK181497 HPM-6000UFBTL Industries, Inc. · 2018
  11. Descendant · cites it directly · 1 of its ownK182022 ApexMVIncontrol Medical, LLC · 2019
  12. Descendant · 2 generations on · 0 of its ownK262353 BTL-299-FBTL Industries, Inc. · 2026
  13. Descendant · 2 generations on · 0 of its ownK252601 Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L)…Hunan Accurate Bio-Medical Technology Co., Ltd. · 2026
  14. Descendant · 2 generations on · 0 of its ownK252334 PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER…Pontemedag · 2026

Showing 5 of 10 descendants. See all descendants

Descendants cleared per year

2015: 12018: 12019: 12023: 22025: 22026: 3
2015high 3 (2026) · low 0 (2016)2026

Most influential descendants

Showing 5 of 10 · See all
  • K181497HPM-6000UFBTL Industries, Inc. · 2018 · cites it directly6descendants
  • K182022ApexMVIncontrol Medical, LLC · 2019 · cites it directly1descendant
  • K262353BTL-299-FBTL Industries, Inc. · 2026 · 2 generations on0descendants
  • K252601Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L); Pelvic Muscle Trainer…Hunan Accurate Bio-Medical Technology Co., Ltd. · 2026 · 2 generations on0descendants
  • K252334PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER PelvicFMS) (033-0-1100-02)Pontemedag · 2026 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K930530Incare PRS 9300 Pelvic FL Thera Syst/Treat Uri IncHollister, Inc.1995—
−7K961872Incare Pelvic Floor Therapy System with Desktop ComputerHollister, Inc.1996—
−6K974048Incare Pelvic Floor Therapy System with Desktop ComputerHollister, Inc.1997—
−5K013612Incare Pelvic Floor Therapy SystemHollister, Inc.2002—
−4K050483Evadri Bladder Control SystemsHollister, Inc.2005—
−3K053434Myotrac Infiniti Electrical StimulatorThought Technology, Ltd.2006—
−2K080950Stiwell MED4Otto Bock, Austria GmbH2009—
−1K110179IncontrolIncontrol Medical, LLC2012—
0 (this device)K134020IntonemvIncontrol Medical, LLC2014—
+1K181497HPM-6000UFBTL Industries, Inc.2018—
+1K182022ApexMVIncontrol Medical, LLC2019—
+2K262353BTL-299-FBTL Industries, Inc.2026—
+2K252601Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L); Pelvic Muscle…Hunan Accurate Bio-Medical Technology Co., Ltd.2026—
+2K252334PELVIPOWER Pelvic Functional Magnetic Stimulation (PELVIPOWER PelvicFMS)…Pontemedag2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198110
198610
198710
199410
199610
199710
199810
200020
200130
200330
200420

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201810
201910
202320
202520
202630
FIG. 1 — Lineage of K134020, 1995–2026Source: 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 KPI? 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 KPI device

  1. #1 K262353 BTL-299-Fscore 14.8 · 10 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

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
*K110179Incontrol
Summary page 1
…Product Code - Manufacturer InControl Medical, LLC K110179 InTone KPI 3225 Gateway Road, Ste. 250 ____…
Incontrol Medical, LLC2012—
*K050483Evadri Bladder Control Systems
Summary page 1
…______________Brookfield,_WI_53045_USA evadi BldderHOLLISTER, Inc. K050483 evadril Bladers KPI 2000 Hollister Dr. Contrl…
Hollister, Inc.2005—

Also cleared against K110179: 6 other devices →

What descends from it? (10)

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

NumberDeviceApplicantDecidedDescendants
K181497HPM-6000UFBTL Industries, Inc.20186
K182022ApexMVIncontrol Medical, LLC20191
K150180InToneIncontrol Medical, LLC20150

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 19 years and passes through 4 companies; a new generation was cleared every 2.9 years on median.
  • None of the 25 ancestors has a recall.
  • Of its descendants, K181497 (BTL Industries, Inc., 2018) has gone furthest, with 6 descendants of its own.
  • 6 other devices also cite its predicate K110179.

How does its category compare?

All KPI devices

KPI Stimulator, Electrical, Non-Implantable, For Incontinence: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · KPI

7so far in 2026, the most since 2007

2007: 12008: 12009: 22011: 12012: 22013: 12014: 32015: 62016: 32017: 12018: 32019: 22020: 12021: 32022: 32023: 32024: 42025: 42026 (partial year): 7
2007high 7 (2026) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KPI

263in 2025

2014: 57 days median2015: 260 days median2016: 89 days median2018: 304 days median2021: 217 days median2022: 181 days median2023: 197 days median2024: 172 days median2025: 263 days median2026 (partial year): 248 days median
2007high 304 (2018) · low 57 (2014)2026

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

Recalls per year · KPI

No recall names KPI since 2007.

Adverse event reports per year · KPI

2in 2024

2013: 12015: 22017: 42019: 22020: 32021: 12022: 22023: 62024: 2
2007high 6 (2023) · low 0 (2007)2025

MAUDE reports naming product code KPI, 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
20071—00
20081—00
20092—00
20100—00
20111—00
20122—00
20131—01
201435700
2015626002
201638900
20171—04
2018330400
20192—02
20201—03
2021321701
2022318102
2023319706
2024417202
2025426300
202672480—

What is it indicated for?

InToneMV is intended to provide electrical stimulation and/or visual biofeedback (via manometry) for the treatment of male and female urinary and fecal incontinence.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K134020: Intonemv.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K134020

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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