510(k) Report

510(k) · Cleared

Cleared

ApexM

K150183510(k) TraditionalCleared Apr 9, 201572-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 Apr 9, 2015 as substantially equivalent to K110179 (Incontrol Medical, LLC, 2012) and 1 other predicate after a 72-day review. Its family tree reaches back 9 generations to 1995. 3 later devices descend from it.

Decided
Apr 9, 2015
Review
72 days
Class
Class II
Product code
KPI
Recalls
None
Predicates
2

Its longest line of descent runs back 9 generations to K930530 (1995). 26 ancestors in all, the oldest K813008 (1981). 3 later devices descend from it, 2 citing it directly.

  1. Root · 9 generations backK930530 Incare PRS 9300 Pelvic FL Thera Syst/Treat Uri IncHollister, Inc. · 1995
  2. 5 generations between
  3. 3 generations backK080950 Stiwell MED4Otto Bock, Austria GmbH · 2009
  4. 2 generations backK110179 IncontrolIncontrol Medical, LLC · 2012
  5. 1 generation backK141158 APEXIncontrol Medical, LLC · 2014
  6. This deviceK150183 ApexMIncontrol Medical, LLC · 2015
  7. Descendant · cites it directly · 1 of its ownK182022 ApexMVIncontrol Medical, LLC · 2019
  8. 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
  9. Descendant · cites it directly · 0 of its ownK163288 Pelvifine Pelvic Muscle TrainerShenzhen Konmed Technology Co., Ltd. · 2018
Show all 9 generations
  1. Root · 9 generations backK930530 Incare PRS 9300 Pelvic FL Thera Syst/Treat Uri IncHollister, Inc. · 1995
  2. 8 generations backK961872 Incare Pelvic Floor Therapy System with Desktop ComputerHollister, Inc. · 1996
  3. 7 generations backK974048 Incare Pelvic Floor Therapy System with Desktop ComputerHollister, Inc. · 1997
  4. 6 generations backK013612 Incare Pelvic Floor Therapy SystemHollister, Inc. · 2002
  5. 5 generations backK050483 Evadri Bladder Control SystemsHollister, Inc. · 2005
  6. 4 generations backK053434 Myotrac Infiniti Electrical StimulatorThought Technology, Ltd. · 2006
  7. 3 generations backK080950 Stiwell MED4Otto Bock, Austria GmbH · 2009
  8. 2 generations backK110179 IncontrolIncontrol Medical, LLC · 2012
  9. 1 generation backK141158 APEXIncontrol Medical, LLC · 2014
  10. This deviceK150183 ApexMIncontrol Medical, LLC · 2015

Most influential descendants

Showing 3 of 3 · See all
  • K182022ApexMVIncontrol Medical, LLC · 2019 · cites it directly1descendant
  • K252601Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L); Pelvic Muscle Trainer…Hunan Accurate Bio-Medical Technology Co., Ltd. · 2026 · 2 generations on0descendants
  • K163288Pelvifine Pelvic Muscle TrainerShenzhen Konmed Technology Co., Ltd. · 2018 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K930530Incare PRS 9300 Pelvic FL Thera Syst/Treat Uri IncHollister, Inc.1995—
−8K961872Incare Pelvic Floor Therapy System with Desktop ComputerHollister, Inc.1996—
−7K974048Incare Pelvic Floor Therapy System with Desktop ComputerHollister, Inc.1997—
−6K013612Incare Pelvic Floor Therapy SystemHollister, Inc.2002—
−5K050483Evadri Bladder Control SystemsHollister, Inc.2005—
−4K053434Myotrac Infiniti Electrical StimulatorThought Technology, Ltd.2006—
−3K080950Stiwell MED4Otto Bock, Austria GmbH2009—
−2K110179IncontrolIncontrol Medical, LLC2012—
−1K141158APEXIncontrol Medical, LLC2014—
0 (this device)K150183ApexMIncontrol Medical, LLC2015—
+1K182022ApexMVIncontrol Medical, LLC2019—
+2K252601Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L); Pelvic Muscle…Hunan Accurate Bio-Medical Technology Co., Ltd.2026—
+1K163288Pelvifine Pelvic Muscle TrainerShenzhen Konmed Technology Co., Ltd.2018—

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
201810
201910
202610
FIG. 1 — Lineage of K150183, 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 4
…Name Product Code Manufacturer InControl Medical, LLC K110179 InTone KPI 3225 Gateway Road, Ste. 250…
Incontrol Medical, LLC2012—
*K141158APEX
Summary page 4
…Brookfield, WI 53045 USA InControl Medical, LLC K141158 Apex KPI 3225 Gateway Road, Ste. 250…
Incontrol Medical, LLC2014—
†K134020IntonemvIncontrol Medical, LLC2014—
†K131420Petite Basic System 701 EltMego Afek AC, Ltd.2013—

Also cleared against K110179: 6 other devices →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K182022ApexMVIncontrol Medical, LLC20191
K163288Pelvifine Pelvic Muscle TrainerShenzhen Konmed Technology Co., Ltd.20180

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 20 years and passes through 4 companies; a new generation was cleared every 2.8 years on median.
  • None of the 26 ancestors has a recall.
  • Of its descendants, K182022 (Incontrol Medical, LLC, 2019) has gone furthest, with 1 descendant 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. 2015, 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?

ApexM is a non-implanted muscle stimulator designed to treat stress, urge and/or mixed urinary incontinence in women. It applies stimulation to the pelvic floor muscles and surrounding structures to improve strength and support.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K150183: ApexM.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K150183

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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