510(k) Report

510(k) · Cleared

Cleared

imani i2Plus Breast Pump

K222573510(k) TraditionalCleared Mar 3, 2023190-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

Imani Co. · HGX Pump, Breast, Powered

Cleared on Mar 3, 2023 as substantially equivalent to K202045 (Imani Co., 2021) after a 190-day review. Its family tree reaches back 8 generations to 1985.

Decided
Mar 3, 2023
Review
190 days
Class
Class II
Product code
HGX
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K850705 (1985). 11 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 8 generations backK850705 The White River Porta-Elec-Breast PumpNatural Technologies, Inc. · 1985
  2. 7 generations backK971543 Luxmatic 12-15 Isc Portable Electric Breast PumpKaweco GmbH · 1997
  3. 6 generations backK012275 PJ.S Comfort Portable Electric Breast PumpLimerick, Inc. · 2002
  4. 5 generations backK051926 Limerick PJ'S Comfort JR Portable Electric Breast PumpLimerick, Inc. · 2005
  5. 4 generations backK150476 Spectra S1Plus and Spectra S2 PlusUzinmedicare Co. · 2016
  6. 3 generations backK180075 MINUET LCD, MINUET LCD ecoUnimom.Co · 2018
  7. 2 generations backK190810 OPERA, OPERA ecoUnimom.Co · 2019
  8. 1 generation backK202045 imani i1Imani Co. · 2021
  9. This deviceK222573 imani i2Plus Breast PumpImani Co. · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K850705The White River Porta-Elec-Breast PumpNatural Technologies, Inc.1985—
−7K971543Luxmatic 12-15 Isc Portable Electric Breast PumpKaweco GmbH1997—
−6K012275PJ.S Comfort Portable Electric Breast PumpLimerick, Inc.2002—
−5K051926Limerick PJ'S Comfort JR Portable Electric Breast PumpLimerick, Inc.2005—
−4K150476Spectra S1Plus and Spectra S2 PlusUzinmedicare Co.2016—
−3K180075MINUET LCD, MINUET LCD ecoUnimom.Co2018—
−2K190810OPERA, OPERA ecoUnimom.Co2019—
−1K202045imani i1Imani Co.2021—
0 (this device)K222573imani i2Plus Breast PumpImani Co.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199510
199710
FIG. 1 — Lineage of K222573, 1985–2023Source: 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
Get a 510(k) Report

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
*K202045imani i1
Summary page 4
…) Regulatory Class: Class II 5. Predicate Device Information Device Name: imani i2 510(k) Number: K202045 Manufacturer: Imani Co. The predicate device has not been subject to a design-related recall. 6. Dev…
Imani Co.2021—

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 38 years and passes through 6 companies; a new generation was cleared every 3.9 years on median.
  • 2 of the 11 ancestors have a recall of any class.

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 imani i2Plus Breast Pump is a powered breast pump to be used by lactating women to express and collect milk from

their breast. The imani i2Plus Breast Pump is a single user device.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K222573: imani i2Plus Breast Pump.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K222573

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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