510(k) Report

510(k) · Cleared

Cleared

MilkMate Breast Pump

K223084510(k) TraditionalCleared Mar 16, 2023167-day reviewClass II21 CFR 884.5160

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

Milkmate Products, Inc. · HGX Pump, Breast, Powered

Cleared on Mar 16, 2023 as substantially equivalent to K201152 (Guangdong Horigen Mother & Baby Products Co., Ltd., 2021) after a 167-day review. Its family tree reaches back 7 generations to 1985. 1 later device descends from it.

Decided
Mar 16, 2023
Review
167 days
Class
Class II
Product code
HGX
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K850705 (1985). 10 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 7 generations backK850705 The White River Porta-Elec-Breast PumpNatural Technologies, Inc. · 1985
  2. 6 generations backK971543 Luxmatic 12-15 Isc Portable Electric Breast PumpKaweco GmbH · 1997
  3. 5 generations backK012275 PJ.S Comfort Portable Electric Breast PumpLimerick, Inc. · 2002
  4. 4 generations backK051926 Limerick PJ'S Comfort JR Portable Electric Breast PumpLimerick, Inc. · 2005
  5. 3 generations backK150476 Spectra S1Plus and Spectra S2 PlusUzinmedicare Co. · 2016
  6. 2 generations backK181784 Spectra S3 PlusUzinmedicare Co. · 2018
  7. 1 generation backK201152 Electric Breast PumpGuangdong Horigen Mother & Baby Products Co., Ltd. · 2021
  8. This deviceK223084 MilkMate Breast PumpMilkmate Products, Inc. · 2023
  9. Descendant · cites it directly · 0 of its ownK241705 MilkMate Breast Pump (A0006); MilkMate Kit (sterile, single-use…Milkmate Products, Inc. · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K241705MilkMate Breast Pump (A0006); MilkMate Kit (sterile, single-use only), 21 mm breast…Milkmate Products, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K850705The White River Porta-Elec-Breast PumpNatural Technologies, Inc.1985—
−6K971543Luxmatic 12-15 Isc Portable Electric Breast PumpKaweco GmbH1997—
−5K012275PJ.S Comfort Portable Electric Breast PumpLimerick, Inc.2002—
−4K051926Limerick PJ'S Comfort JR Portable Electric Breast PumpLimerick, Inc.2005—
−3K150476Spectra S1Plus and Spectra S2 PlusUzinmedicare Co.2016—
−2K181784Spectra S3 PlusUzinmedicare Co.2018—
−1K201152Electric Breast PumpGuangdong Horigen Mother & Baby Products Co., Ltd.2021—
0 (this device)K223084MilkMate Breast PumpMilkmate Products, Inc.2023—
+1K241705MilkMate Breast Pump (A0006); MilkMate Kit (sterile, single-use only), 21 mm…Milkmate Products, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199510
199710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K223084, 1985–2024Source: 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 HGX? 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 HGX device

  1. #1 K212180 Wearable Breast Pump (Model S12)score 34.9 · 8 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
*K201152Electric Breast Pump
Summary page 5
…223084 Page 2 of 8 PREDICATE DEVICE: Electric Breast Pump, Model XN/MS-2224B (K201152) The predicate device has not been subject to a design-related recall. DEVICE DESCRIPTION: The MilkMate Breast Pump includes a…
Guangdong Horigen Mother & Baby Products Co., Ltd.2021—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K241705MilkMate Breast Pump (A0006); MilkMate Kit (sterile, single-use only), 21 mm breast…Milkmate Products, Inc.20240

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 38 years and passes through 6 companies; a new generation was cleared every 3.9 years on median.
  • 2 of the 10 ancestors have a recall of any class.
  • Of its descendants, K241705 (Milkmate Products, Inc., 2024) has gone furthest, with 0 descendants of its own.

How does its category compare?

All HGX devices

HGX Pump, Breast, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · HGX

34so far in 2026, the most since 2007

2007: 12008: 22009: 42010: 72011: 22012: 62013: 42014: 32015: 92016: 72017: 82018: 62019: 72020: 92021: 122022: 152023: 152024: 192025: 262026 (partial year): 34
2007high 34 (2026) · low 1 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HGX

122in 2025

2009: 121 days median2010: 103 days median2012: 180 days median2013: 131 days median2014: 120 days median2015: 141 days median2016: 121 days median2017: 159 days median2018: 136 days median2019: 158 days median2020: 128 days median2021: 240 days median2022: 190 days median2023: 167 days median2024: 168 days median2025: 122 days median2026 (partial year): 142 days median
2007high 240 (2021) · low 103 (2010)2026

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

Recalls per year · HGX

1in 2017

2010: 52011: 12017: 1
2007high 5 (2010) · low 0 (2007)2026

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

Adverse event reports per year · HGX

69in 2025

2007: 22008: 22010: 882011: 2402012: 6852013: 8372014: 1,0362015: 4962016: 3732017: 4372018: 2912019: 1682020: 1682021: 1192022: 1542023: 2002024: 1182025: 69
2007high 1,036 (2014) · low 0 (2009)2025

MAUDE reports naming product code HGX, 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—02
20082—02
2009412100
20107103588
20112—1240
201261800685
201341310837
2014312001,036
201591410496
201671210373
201781591437
201861360291
201971580168
202091280168
2021122400119
2022151900154
2023151670200
2024191680118
202526122069
2026341420—

What is it indicated for?

The MilkMate Breast Pump is intended to be used by lactating women to express and collect milk from their breast, to alleviate engorgement of the breast, maintain the ability of lactation, and provide mother's milk for future feedings when separation of mother and baby occurs. It is intended for multiple users in places of work, shared spaces, healthcare facilities, hospitals, and the home.

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. “K223084: MilkMate Breast Pump.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K223084

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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