510(k) Report

510(k) · Cleared

Cleared

Mint ACE Pump

K260001510(k) TraditionalCleared Sep 11, 2026252-day reviewClass II21 CFR 880.5730

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

Beta Bionics, Inc. · QFG Alternate Controller Enabled Insulin Infusion Pump

Cleared on Sep 11, 2026 as substantially equivalent to K231826 (Insulet Corporation, 2023) after a 252-day review. Its family tree reaches back 4 generations to 2019. 1 of the 5 devices in its family, counting itself, has a Class I recall.

Decided
Sep 11, 2026
Review
252 days
Class
Class II
Product code
QFG
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to DEN180058 (2019). No later device cites it as a predicate yet. 1 of the 5 devices in this family, counting this one, has a Class I recall.

  1. Root · 4 generations backDEN180058 t:slim X2 insulin pump with interoperable technologyTandem Diabetes Care, Inc. · 2019
  2. 3 generations backK191679 Omnipod DASH Insulin Management System with interoperable technologyInsulet Corporation · 2019
  3. 2 generations backK203768 Omnipod 5 ACE Pump (Pod)Insulet Corporation · 2022 · Recalled
  4. 1 generation backK231826 Omnipod 5 ACE PumpInsulet Corporation · 2023 · Recalled (Class I)
  5. This deviceK260001 Mint ACE PumpBeta Bionics, Inc. · 2026

Class I recalls in this family

View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4DEN180058t:slim X2 insulin pump with interoperable technologyTandem Diabetes Care, Inc.2019—
−3K191679Omnipod DASH Insulin Management System with interoperable technologyInsulet Corporation2019—
−2K203768Omnipod 5 ACE Pump (Pod)Insulet Corporation20222
−1K231826Omnipod 5 ACE PumpInsulet Corporation2023Class I
0 (this device)K260001Mint ACE PumpBeta Bionics, Inc.2026—
FIG. 1 — Lineage of K260001, 2019–2026Source: 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.

1 device in this family has a Class I recall. 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 QFG device

  1. #1 K251032 MiniMed 780G insulin pumpscore 19.6 · 11 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
*K231826Omnipod 5 ACE Pump
Summary page 5
…p) Classification Name: Alternate controller enabled infusion pump (21 CFR 880.5730, QFG) Predicate Devices Omnipod 5 (Insulet Corporation, 510(k) K231826) Description of the Mint ACE Pump The Beta Bionics Mint System consists of the Mint pump (Mint ACE Pump preinstalled wit…
Insulet Corporation2023Class I

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K231826Omnipod 5 ACE PumpInsulet Corporation · 2023 · Direct predicate · ◆ on the line of descent in FIG. 13 Class I recalls

What does this lineage say?

  • The line of descent spans 7 years and passes through 3 companies; a new generation was cleared every 2.4 years on median.
  • 2 of the 4 ancestors have a recall of any class; 1 has a Class I recall.

How does its category compare?

All QFG devices

QFG Alternate Controller Enabled Insulin Infusion Pump: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · QFG

5in 2025

2019: 22020: 12022: 22023: 92024: 52025: 52026 (partial year): 6
2007high 9 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QFG

44in 2025

2023: 150 days median2024: 89 days median2025: 44 days median2026 (partial year): 103 days median
2007high 150 (2023) · low 44 (2025)2026

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

Recalls per year · QFG

8so far in 2026, the most since 2007

2022: 12023: 1, 1 Class I2025: 3, 1 Class I2026 (partial year): 8, 1 Class I
2007high 8 (2026) · low 0 (2007)2026

Class I (3 since 2007) Class II/III not classified

Adverse event reports per year · QFG

324,360in 2025

2020: 30,5222021: 74,7012022: 129,1192023: 188,0142024: 273,1802025: 324,360
2007high 324,360 (2025) · low 0 (2007)2025

MAUDE reports naming product code QFG, 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
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20192—00
20201—030,522
20210—074,701
20222—1129,119
202391501 (1)188,014
20245890273,180
20255443 (1)324,360
202661038 (1)—

What is it indicated for?

The Mint ACE Pump (Mint pump) is intended for the subcutaneous delivery of insulin for the management of diabetes mellitus in persons requiring insulin. The Mint pump is able to reliably and securely communicate with compatible, digitally connected devices, including automated insulin dosing software, to receive, execute, and confirm commands from these devices. The Mint ACE Pump is intended for the management of diabetes mellitus in people 6 years of age or older. The Mint pump is intended for single-person, home use and requires a prescription.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K260001: Mint ACE Pump.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K260001

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Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026