510(k) Report

510(k) · Cleared

Cleared

eMVFit (MVF-10M)

K240992510(k) TraditionalCleared Oct 10, 2024182-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

Weero Co., Ltd. · IPF Stimulator, Muscle, Powered

Cleared on Oct 10, 2024 as substantially equivalent to K210877 (InMode, Ltd., 2021) and 2 other predicates after a 182-day review. Its family tree reaches back 25 generations to 1995.

Decided
Oct 10, 2024
Review
182 days
Class
Class II
Product code
IPF
Recalls
None
Predicates
3

Its longest line of descent runs back 25 generations to K943450 (1995). 344 ancestors in all, the oldest K800617 (1980). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2021: 1 other ancestor2019: 1 other ancestor2015: 1 other ancestor2014: 1 other ancestor2013: 1 other ancestor2011: 3 other ancestors2008: 2 other ancestors2009: 5 other ancestors2007: 6 other ancestors2004: 17 other ancestors2002: 35 other ancestors1997: 24 other ancestors2005: 11 other ancestors2000: 26 other ancestors1996: 21 other ancestors1995: 17 other ancestors1993: 11 other ancestors2003: 25 other ancestors2001: 28 other ancestors1998: 21 other ancestors1991: 10 other ancestors1985: 2 other ancestors1986: 3 other ancestors2012: 1 other ancestor1994: 15 other ancestors2010: 2 other ancestors2006: 3 other ancestors1999: 12 other ancestors1990: 3 other ancestors1980: 1 other ancestor1992: 4 other ancestors1984: 1 other ancestor1989: 3 other ancestors1988: 1 other ancestor1982: 1 other ancestorK943450 · Arthrocare Arthroscopic Electrosurgery System Model 970 · Arthrocare Corp. · 1995×2: 2 generations cleared close together, K961069 (1996), K962445 (1996) K964849 · Arthrocare Dermatologic Electrosurgery System · Arthrocare Corp. · 1997K973478 · Arthrocare Sinus Electrosurgery System · Arthrocare Corp. · 1998K981870 · Visage Cosmetic Surgery System · Arthrocare Corp. · 1998K000944 · Thermage Thermacool System · Thermage, Inc. · 2000×2: 2 generations cleared close together, K013034 (2001), K013639 (2002) ×2: 2 generations cleared close together, K021402 (2002), K030142 (2003) K031671 · Polaris WR · Syneron Medical, Ltd. · 2003K051214 · Aluma Skin Renewal System · Lumenis, Inc. · 2005K060448 · Lumenis One Family of Systems; Lumenis One. · Lumenis, Ltd. · 2006×2: 2 generations cleared close together, K072564 (2008), K082876 (2008) K111303 · Dermatological Treatment Device Family · Sharplight Technologies, Ltd. · 2011K133837 · Viora V-Total · Viora, Ltd. · 2014×2: 2 generations cleared close together, K142093 (2014), K150035 (2015) K153568 · InMode Plus System · Inmode MD, Ltd. · 2016K172302 · InMode PLUS System · Inmode MD, Ltd. · 2017K183450 · EmBody System · Inmode MD, Ltd. · 2019×2: 2 generations cleared close together, K201285 (2021), K210877 (2021) 19801990200020102020
Other ancestors, by generation 1 generation back: 1 other ancestor2 generations back: 2 other ancestors3 generations back: 4 other ancestors4 generations back: 9 other ancestors5 generations back: 14 other ancestors6 generations back: 14 other ancestors7 generations back: 4 other ancestors8 generations back: 6 other ancestors9 generations back: 13 other ancestors10 generations back: 41 other ancestors11 generations back: 97 other ancestors12 generations back: 65 other ancestors13 generations back: 31 other ancestors14 generations back: 11 other ancestors15 generations back: 5 other ancestors16 generations back: 2 other ancestors K210877 · Evolve System with the T3 Applicator · InMode, Ltd. · 2021K201285 · InMode Evolve System with the Tone Applicator · InMode, Ltd. · 2021K183450 · EmBody System · Inmode MD, Ltd. · 2019K172302 · InMode PLUS System · Inmode MD, Ltd. · 2017K153568 · InMode Plus System · Inmode MD, Ltd. · 2016K150035 · V10 system · Viora, Ltd. · 2015K142093 · V20 System · Viora, Ltd. · 2014K133837 · Viora V-Total · Viora, Ltd. · 2014K111303 · Dermatological Treatment Device Family · Sharplight Technologies, Ltd. · 2011K082876 · Beamax/ Formax Pulsed Light Device Family · Sharplight Technologies, Ltd. · 2008K072564 · Alma Lasers Harmony XL Multi-Application Platform · Alma Lasers, Ltd. · 2008K060448 · Lumenis One Family of Systems; Lumenis One. · Lumenis, Ltd. · 2006K051214 · Aluma Skin Renewal System · Lumenis, Inc. · 2005K031671 · Polaris WR · Syneron Medical, Ltd. · 2003K030142 · Thermacool TC System · Thermage, Inc. · 2003K021402 · Thermage Thermacool TC System · Thermage, Inc. · 2002K013639 · Thermage Thermacool TC System · Thermage, Inc. · 2002K013034 · Modification to: Thermacool Iia · Thermage, Inc. · 2001K000944 · Thermage Thermacool System · Thermage, Inc. · 2000K981870 · Visage Cosmetic Surgery System · Arthrocare Corp. · 1998K973478 · Arthrocare Sinus Electrosurgery System · Arthrocare Corp. · 1998K964849 · Arthrocare Dermatologic Electrosurgery System · Arthrocare Corp. · 1997K962445 · Arthrocare Dental Electrosurgery System · Arthrocare Corp. · 1996K961069 · Arthrocare Urologic Multi-Electrode Electrosurgery System · Arthrocare Corp. · 1996K943450 · Arthrocare Arthroscopic Electrosurgery System Model 970 · Arthrocare Corp. · 1995−25−20−15−10−50
  1. Root · 25 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 21 generations between
  3. 3 generations backK183450 EmBody SystemInmode MD, Ltd. · 2019
  4. 2 generations backK201285 InMode Evolve System with the Tone ApplicatorInMode, Ltd. · 2021
  5. 1 generation backK210877 Evolve System with the T3 ApplicatorInMode, Ltd. · 2021
  6. This deviceK240992 eMVFit (MVF-10M)Weero Co., Ltd. · 2024
Show all 25 generations
  1. Root · 25 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 24 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
  3. 23 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
  4. 22 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
  5. 21 generations backK973478 Arthrocare Sinus Electrosurgery SystemArthrocare Corp. · 1998
  6. 20 generations backK981870 Visage Cosmetic Surgery SystemArthrocare Corp. · 1998
  7. 19 generations backK000944 Thermage Thermacool SystemThermage, Inc. · 2000
  8. 18 generations backK013034 Modification to: Thermacool IiaThermage, Inc. · 2001
  9. 17 generations backK013639 Thermage Thermacool TC SystemThermage, Inc. · 2002
  10. 16 generations backK021402 Thermage Thermacool TC SystemThermage, Inc. · 2002
  11. 15 generations backK030142 Thermacool TC SystemThermage, Inc. · 2003
  12. 14 generations backK031671 Polaris WRSyneron Medical, Ltd. · 2003
  13. 13 generations backK051214 Aluma Skin Renewal SystemLumenis, Inc. · 2005
  14. 12 generations backK060448 Lumenis One Family of Systems; Lumenis One.Lumenis, Ltd. · 2006
  15. 11 generations backK072564 Alma Lasers Harmony XL Multi-Application PlatformAlma Lasers, Ltd. · 2008
  16. 10 generations backK082876 Beamax/ Formax Pulsed Light Device FamilySharplight Technologies, Ltd. · 2008
  17. 9 generations backK111303 Dermatological Treatment Device FamilySharplight Technologies, Ltd. · 2011
  18. 8 generations backK133837 Viora V-TotalViora, Ltd. · 2014
  19. 7 generations backK142093 V20 SystemViora, Ltd. · 2014
  20. 6 generations backK150035 V10 systemViora, Ltd. · 2015
  21. 5 generations backK153568 InMode Plus SystemInmode MD, Ltd. · 2016
  22. 4 generations backK172302 InMode PLUS SystemInmode MD, Ltd. · 2017
  23. 3 generations backK183450 EmBody SystemInmode MD, Ltd. · 2019
  24. 2 generations backK201285 InMode Evolve System with the Tone ApplicatorInMode, Ltd. · 2021
  25. 1 generation backK210877 Evolve System with the T3 ApplicatorInMode, Ltd. · 2021
  26. This deviceK240992 eMVFit (MVF-10M)Weero Co., Ltd. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−25K943450Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp.1995—
−24K961069Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp.1996—
−23K962445Arthrocare Dental Electrosurgery SystemArthrocare Corp.1996—
−22K964849Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp.1997—
−21K973478Arthrocare Sinus Electrosurgery SystemArthrocare Corp.1998—
−20K981870Visage Cosmetic Surgery SystemArthrocare Corp.1998—
−19K000944Thermage Thermacool SystemThermage, Inc.2000—
−18K013034Modification to: Thermacool IiaThermage, Inc.2001—
−17K013639Thermage Thermacool TC SystemThermage, Inc.2002—
−16K021402Thermage Thermacool TC SystemThermage, Inc.2002—
−15K030142Thermacool TC SystemThermage, Inc.2003—
−14K031671Polaris WRSyneron Medical, Ltd.2003—
−13K051214Aluma Skin Renewal SystemLumenis, Inc.2005—
−12K060448Lumenis One Family of Systems; Lumenis One.Lumenis, Ltd.2006—
−11K072564Alma Lasers Harmony XL Multi-Application PlatformAlma Lasers, Ltd.2008—
−10K082876Beamax/ Formax Pulsed Light Device FamilySharplight Technologies, Ltd.2008—
−9K111303Dermatological Treatment Device FamilySharplight Technologies, Ltd.2011—
−8K133837Viora V-TotalViora, Ltd.2014—
−7K142093V20 SystemViora, Ltd.2014—
−6K150035V10 systemViora, Ltd.2015—
−5K153568InMode Plus SystemInmode MD, Ltd.2016—
−4K172302InMode PLUS SystemInmode MD, Ltd.2017—
−3K183450EmBody SystemInmode MD, Ltd.2019—
−2K201285InMode Evolve System with the Tone ApplicatorInMode, Ltd.2021—
−1K210877Evolve System with the T3 ApplicatorInMode, Ltd.2021—
0 (this device)K240992eMVFit (MVF-10M)Weero Co., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
198210
198410
198520
198630
198810
198930
199030
1991100
199240
1993110
1994150
1995170
1996210
1997240
1998210
1999120
2000260
2001280
2002350
2003250
2004170
2005110
200630
200760
200820
200950
201020
201130
201210
201310
201410
201510
201910
202110
FIG. 1 — Lineage of K240992, 1995–2024Source: 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
Get a 510(k) Report

What was it cleared against? (3)

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
*K210877Evolve System with the T3 Applicator
Summary page 6
…INMODE LTD. INMODE LTD. TimeWaver Production GmbH 510(k) No. - K210877 K201285 K212832…
InMode, Ltd.2021—
*K201285InMode Evolve System with the Tone Applicator
Summary page 5
…Device 510(k) No. Main Predicate INMODE LTD. Evolve System with the T3 Applicator K201285 Reference Predicate INMODE LTD. Evolve System with the Tone Applicator K201285 Time…
InMode, Ltd.2021—
*K212832TimeWaver Frequency
Summary page 5
…Evolve System with the Tone Applicator K201285 TimeWaver TimeWaver Frequency K212832 Production GmbH 4. Description of the Device eMVFit has MULTI handpiece, EMS handpiece, patient switch, cradle, distill…
Timewaver Production GmbH2021—

Also cleared against K210877: 4 other devices →

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 29 years and passes through 11 companies; a new generation was cleared every 10 months on median.
  • 11 of the 344 ancestors have a recall of any class.
  • 4 other devices also cite its predicate K210877.

How does its category compare?

All IPF devices

IPF Stimulator, Muscle, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, 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?

EMS is used for:

* Relaxation of muscle spasms

* Prevention or retardation of disuse atrophy

* Increasing local blood circulation

* Muscle re-education

* Maintaining or increasing range of motion

* Immediate postsurgical stimulation of calf muscles to prevent venous thrombosis

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K240992: eMVFit (MVF-10M).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K240992

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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