510(k) Report

510(k) · Cleared

Recalled · Class II · 2025

Dexcom G7 Continuous Glucose Monitoring (CGM) System

K231081510(k) SpecialCleared May 15, 202328-day reviewClass II21 CFR 862.1355Recalls 1

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

Dexcom, Inc. · QBJ Integrated Continuous Glucose Monitoring System, Factory Calibrated

Cleared on May 15, 2023 as substantially equivalent to K213919 (Dexcom, Inc., 2022) after a 28-day review. Its family tree reaches back 6 generations to 2018. 1 of the 20 devices in its family, counting itself, has a Class I recall. 11 later devices descend from it. It has been recalled once.

Decided
May 15, 2023
Review
28 days
Class
Class II
Product code
QBJ
Recalls
1
Predicates
1

Its longest line of descent runs back 6 generations to DEN170088 (2018). 8 ancestors in all. 11 later devices descend from it, 2 citing it directly. 1 of the 20 devices in this family, counting this one, has a Class I recall.

  1. Root · 6 generations backDEN170088 Dexcom G6 Continuous Glucose Monitoring SystemDexcom, Inc. · 2018
  2. 5 generations backK182041 Dexcom G6 Glucose Program Continuous Glucose Monitoring SystemDexcom, Inc. · 2018
  3. 4 generations backK191450 Dexcom G6 Continuous Glucose Monitoring System, Dexcom G6 Glucose…Dexcom, Inc. · 2019 · Recalled
  4. 3 generations backK200876 Dexcom G6 Continuous Glucose Monitoring System, Dexcom G6 Glucose…Dexcom, Inc. · 2020 · Recalled
  5. 2 generations backK201328 Dexcom G6 Continuous Glucose Monitoring (CGM) SystemDexcom, Inc. · 2021
  6. 1 generation backK213919 Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2022 · Recalled (Class I)
  7. This deviceK231081 Dexcom G7 Continuous Glucose Monitoring (CGM) SystemDexcom, Inc. · 2023
  8. Descendant · cites it directly · 5 of its ownK234133 Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2024
  9. Descendant · 2 generations on · 4 of its ownK240902 Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2024 · Recalled
  10. Descendant · cites it directly · 4 of its ownK234070 Stelo Glucose Biosensor SystemDexcom, Inc. · 2024
  11. Descendant · 3 generations on · 3 of its ownK243214 Dexcom G7 15 Day Continuous Glucose Monitoring SystemDexcom, Inc. · 2025 · Recalled
  12. Descendant · 2 generations on · 1 of its ownK260935 Stelo Glucose Biosensor SystemDexcom, Inc. · 2026

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2024: 32025: 32026: 5
2024high 5 (2026) · low 3 (2024)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 11 · See all
  • K234133Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2024 · cites it directly5descendants
  • K240902Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2024 · 2 generations on4descendants
  • K234070Stelo Glucose Biosensor SystemDexcom, Inc. · 2024 · cites it directly4descendants
  • K243214Dexcom G7 15 Day Continuous Glucose Monitoring SystemDexcom, Inc. · 2025 · 3 generations on3descendants
  • K260935Stelo Glucose Biosensor SystemDexcom, Inc. · 2026 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6DEN170088Dexcom G6 Continuous Glucose Monitoring SystemDexcom, Inc.2018—
−5K182041Dexcom G6 Glucose Program Continuous Glucose Monitoring SystemDexcom, Inc.2018—
−4K191450Dexcom G6 Continuous Glucose Monitoring System, Dexcom G6 Glucose Program…Dexcom, Inc.20192
−3K200876Dexcom G6 Continuous Glucose Monitoring System, Dexcom G6 Glucose Program…Dexcom, Inc.20201
−2K201328Dexcom G6 Continuous Glucose Monitoring (CGM) SystemDexcom, Inc.2021—
−1K213919Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc.2022Class I
0 (this device)K231081Dexcom G7 Continuous Glucose Monitoring (CGM) SystemDexcom, Inc.2023—
+1K234133Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc.2024—
+2K240902Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc.20243
+1K234070Stelo Glucose Biosensor SystemDexcom, Inc.2024—
+3K243214Dexcom G7 15 Day Continuous Glucose Monitoring SystemDexcom, Inc.20252
+2K260935Stelo Glucose Biosensor SystemDexcom, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201810
201910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202430
202530
202650
FIG. 1 — Lineage of K231081, 2018–2026Source: 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 QBJ device

  1. #1 K253737 Dexcom G7 Continuous Glucose Monitoring (CGM)…score 16.5 · 10 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
*K213919Dexcom G7 Continuous Glucose Monitoring System
Summary page 4
…nel Clinical Chemistry 7.3. Predicate Device The modified device is substantially equivalent to Dexcom G7 Continuous Glucose Monitoring (CGM) System, K213919. The changes described here do not change the intended use or the fundamental scientific technology of the modified device. ===…
Dexcom, Inc.2022Class I

What descends from it? (11)

See all 11

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K234133Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc.20245
K234070Stelo Glucose Biosensor SystemDexcom, Inc.20244

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

Recalls of this device

DateClassRecallRoot causeReason
May 5, 2025Class IIZ-1906-2025Software designA bug in the 2.7.0 version of the G7 iOS App can cause the app to enter a state where it stops updating the estimated glucose value (EGV) and continues to show this stale EGV. If the user is unaware that the EGVs are not being updated and…

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.

  • K213919Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2022 · Direct predicate · ◆ on the line of descent in FIG. 14 Class I recalls

What does this lineage say?

  • The line of descent spans 5 years and passes through 1 company; a new generation was cleared every 8 months on median.
  • 3 of the 8 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K234133 (Dexcom, Inc., 2024) has gone furthest, with 5 descendants of its own.

How does its category compare?

All QBJ devices

QBJ Integrated Continuous Glucose Monitoring System, Factory Calibrated: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · QBJ

2in 2025

2018: 12019: 22020: 12021: 12022: 22023: 42024: 32025: 22026 (partial year): 2
2007high 4 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QBJ

59in 2024

2023: 89 days median2024: 59 days median
2007high 89 (2023) · low 59 (2024)2026

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

Recalls per year · QBJ

4so far in 2026, the most since 2007

2025: 2, 1 Class I2026 (partial year): 4
2007high 4 (2026) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · QBJ

374,651in 2025

2007: 32018: 37,1062019: 80,7742020: 200,7382021: 254,8332022: 232,2882023: 273,5652024: 347,1242025: 374,651
2007high 374,651 (2025) · low 0 (2008)2025

MAUDE reports naming product code QBJ, 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—03
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20181—037,106
20192—080,774
20201—0200,738
20211—0254,833
20222—0232,288
20234890273,565
20243590347,124
20252—2 (1)374,651
20262—4—

What is it indicated for?

The Dexcom G7 Continuous Glucose Monitoring (CGM) System is a real time, continuous glucose monitoring device indicated for the management of diabetes in persons 2 years and older. The Dexcom G7 CGM System is intended to replace fingerstick BG testing for diabetes treatment decisions. Interpretation of the Dexcom G7 CGM System results should be based on the glucose trends and several sequential sensor readings over time. The Dexcom G7 CGM System also…

Read the full statement (134 words)

The Dexcom G7 Continuous Glucose Monitoring (CGM) System is a real time, continuous glucose monitoring device indicated for the management of diabetes in persons 2 years and older.

The Dexcom G7 CGM System is intended to replace fingerstick BG testing for diabetes treatment decisions. Interpretation of the Dexcom G7 CGM System results should be based on the glucose trends and several sequential sensor readings over time. The Dexcom G7 CGM System also aids in the detection of episodes of hyperglycemia and hypoglycemia, facilitating both acute and long-term therapy adjustments.

The Dexcom G7 CGM System is also intended to autonomously communicate with digitally connected devices, including automated insulin dosing (AID) systems. The Dexcom G7 CGM System can be used alone or in conjunction with these digitally connected medical devices for the purposes of managing diabetes.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K231081: Dexcom G7 Continuous Glucose Monitoring (CGM) System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K231081

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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