510(k) Report

510(k) · Cleared

Cleared

MiMo (TM) Negative Pressure Wound Therapy System

K181929510(k) TraditionalCleared Mar 27, 2019252-day reviewClass II21 CFR 878.4780

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

Baymax Research, Inc. · OMP Negative Pressure Wound Therapy Powered Suction Pump

Cleared on Mar 27, 2019 as substantially equivalent to K180840 (Genadyne Biotechnologies, Inc., 2018) after a 252-day review. Its family tree reaches back 11 generations to 1995.

Decided
Mar 27, 2019
Review
252 days
Class
Class II
Product code
OMP
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K945062 (1995). 26 ancestors in all, the oldest K933902 (1994). No later device cites it as a predicate yet.

  1. Root · 11 generations backK945062 VacplusKinetic Concepts, Inc. · 1995
  2. 7 generations between
  3. 3 generations backK151436 PICO Single Use Negative Pressure Wound Therapy SystemSmith & Nephew Medical, Ltd. · 2016
  4. 2 generations backK161599 UNO Negative Pressure Wound Therapy SystemGenadyne Biotechnologies, Inc. · 2017
  5. 1 generation backK180840 UNO Negative Pressure Wound Therapy SystemGenadyne Biotechnologies, Inc. · 2018
  6. This deviceK181929 MiMo (TM) Negative Pressure Wound Therapy SystemBaymax Research, Inc. · 2019
Show all 11 generations
  1. Root · 11 generations backK945062 VacplusKinetic Concepts, Inc. · 1995
  2. 10 generations backK042134 Versatile 1 Wound Vacuum SystemBlue Sky Medical Group Incorporated · 2004 · Recalled
  3. 9 generations backK052456 Modification to Versatile 1 Wound Vacuum SystemBlue Sky Medical Group Incorporated · 2005
  4. 8 generations backK061919 Versatile 1 Ezcare Wound Vacuum SystemBlue Sky Medical Group Incorporated · 2007 · Recalled
  5. 7 generations backK082426 Renasys EZSmith & Nephew, Inc. · 2008 · Recalled
  6. 6 generations backK083375 Renasys GO Negative Pressure Wound TherapySmith & Nephew, Inc. · 2009 · Recalled
  7. 5 generations backK111170 PICOSmith & Nephew, Inc. · 2011
  8. 4 generations backK112127 Pico Single Use Negative Pressure Wound Therapy SystemSmith & Nephew, Inc. · 2012
  9. 3 generations backK151436 PICO Single Use Negative Pressure Wound Therapy SystemSmith & Nephew Medical, Ltd. · 2016
  10. 2 generations backK161599 UNO Negative Pressure Wound Therapy SystemGenadyne Biotechnologies, Inc. · 2017
  11. 1 generation backK180840 UNO Negative Pressure Wound Therapy SystemGenadyne Biotechnologies, Inc. · 2018
  12. This deviceK181929 MiMo (TM) Negative Pressure Wound Therapy SystemBaymax Research, Inc. · 2019
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K945062VacplusKinetic Concepts, Inc.1995—
−10K042134Versatile 1 Wound Vacuum SystemBlue Sky Medical Group Incorporated20042
−9K052456Modification to Versatile 1 Wound Vacuum SystemBlue Sky Medical Group Incorporated2005—
−8K061919Versatile 1 Ezcare Wound Vacuum SystemBlue Sky Medical Group Incorporated20071
−7K082426Renasys EZSmith & Nephew, Inc.20084
−6K083375Renasys GO Negative Pressure Wound TherapySmith & Nephew, Inc.20092
−5K111170PICOSmith & Nephew, Inc.2011—
−4K112127Pico Single Use Negative Pressure Wound Therapy SystemSmith & Nephew, Inc.2012—
−3K151436PICO Single Use Negative Pressure Wound Therapy SystemSmith & Nephew Medical, Ltd.2016—
−2K161599UNO Negative Pressure Wound Therapy SystemGenadyne Biotechnologies, Inc.2017—
−1K180840UNO Negative Pressure Wound Therapy SystemGenadyne Biotechnologies, Inc.2018—
0 (this device)K181929MiMo (TM) Negative Pressure Wound Therapy SystemBaymax Research, Inc.2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199710
199910
200010
200210
200310
200510
200630
200720
200820
201010
FIG. 1 — Lineage of K181929, 1995–2019Source: 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 OMP? 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 OMP device

  1. #1 K260646 Renasys Edge (66803126)score 15.3 · 14 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
*K180840UNO Negative Pressure Wound Therapy System
Cleared while this submission was under review
Summary page 4
…assification Name OMP, Negative Pressure Wound Therapy Powered Suction Pump 21 C.F.R. § 878.4780 Predicate Device Genadyne UNO Negative Pressure Wound Therapy System, K180840 Device Description The MiMo™ Negative Pressure Wound Therapy System is a portable, battery powered wound suction pump with the…
Genadyne Biotechnologies, Inc.2018—

Also cleared against K180840: 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 24 years and passes through 6 companies; a new generation was cleared every 1.3 years on median.
  • 10 of the 26 ancestors have a recall of any class.
  • 1 other device also cites its predicate K180840.

How does its category compare?

All OMP devices

OMP Negative Pressure Wound Therapy Powered Suction Pump: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · OMP

5in 2025

2007: 62008: 82009: 82010: 62011: 62012: 112013: 112014: 102015: 202016: 192017: 112018: 132019: 152020: 62021: 92022: 102023: 82024: 92025: 52026 (partial year): 9
2007high 20 (2015) · low 5 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OMP

127in 2025

2007: 113 days median2008: 98 days median2009: 87 days median2010: 97 days median2011: 123 days median2012: 292 days median2013: 84 days median2014: 179 days median2015: 189 days median2016: 146 days median2017: 137 days median2018: 214 days median2019: 249 days median2020: 179 days median2021: 238 days median2022: 229 days median2023: 291 days median2024: 181 days median2025: 127 days median2026 (partial year): 141 days median
2007high 292 (2012) · low 84 (2013)2026

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

Recalls per year · OMP

2in 2024

2009: 72010: 32012: 12013: 22014: 42015: 12016: 22019: 12024: 2
2007high 7 (2009) · low 0 (2007)2026

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

Adverse event reports per year · OMP

140in 2025

2007: 12008: 12009: 792010: 802011: 1302012: 972013: 1692014: 2292015: 3782016: 3982017: 3682018: 4222019: 9942020: 3,6642021: 1,4222022: 2582023: 1432024: 1352025: 140
2007high 3,664 (2020) · low 1 (2007)2025

MAUDE reports naming product code OMP, 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
2007611301
200889801
2009887779
2010697380
201161230130
201211292197
201311842169
2014101794229
2015201891378
2016191462398
2017111370368
2018132140422
2019152491994
2020617903,664
2021923801,422
2022102290258
202382910143
202491812135
202551270140
202691410—

What is it indicated for?

The MiMo™ Negative Pressure Wound Therapy System is indicated for use in patients who would benefit from negative pressure wound therapy particularly as the device may promote wound healing by the removal of low to moderate exudates and infectious material.

Appropriate wound types include:

- Chronic

- Acute

- Traumatic

- Subacute and dehisced wounds

- Partial-thickness burns

- Ulcers (such as diabetic or pressure)

- Flaps and grafts

- Closed surgical incisions

MiMo™ Negative Pressure Wound Therapy System is a single patient use device.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K181929: MiMo (TM) Negative Pressure Wound Therapy System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K181929

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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