510(k) Report

510(k) · Cleared

Cleared

Dexcom G7 Continuous Glucose Monitoring System

K234133510(k) TraditionalCleared Feb 26, 202459-day reviewClass II21 CFR 862.1355

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 Feb 26, 2024 as substantially equivalent to K231081 (Dexcom, Inc., 2023) after a 59-day review. Its family tree reaches back 7 generations to 2018. 1 of the 15 devices in its family, counting itself, has a Class I recall. 5 later devices descend from it.

Decided
Feb 26, 2024
Review
59 days
Class
Class II
Product code
QBJ
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to DEN170088 (2018). 9 ancestors in all. 5 later devices descend from it, 1 citing it directly. 1 of the 15 devices in this family, counting this one, has a Class I recall.

  1. Root · 7 generations backDEN170088 Dexcom G6 Continuous Glucose Monitoring SystemDexcom, Inc. · 2018
  2. 6 generations backK182041 Dexcom G6 Glucose Program Continuous Glucose Monitoring SystemDexcom, Inc. · 2018
  3. 5 generations backK191450 Dexcom G6 Continuous Glucose Monitoring System, Dexcom G6 Glucose…Dexcom, Inc. · 2019 · Recalled
  4. 4 generations backK200876 Dexcom G6 Continuous Glucose Monitoring System, Dexcom G6 Glucose…Dexcom, Inc. · 2020 · Recalled
  5. 3 generations backK201328 Dexcom G6 Continuous Glucose Monitoring (CGM) SystemDexcom, Inc. · 2021
  6. 2 generations backK213919 Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2022 · Recalled (Class I)
  7. 1 generation backK231081 Dexcom G7 Continuous Glucose Monitoring (CGM) SystemDexcom, Inc. · 2023 · Recalled
  8. This deviceK234133 Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2024
  9. Descendant · cites it directly · 4 of its ownK240902 Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2024 · Recalled
  10. Descendant · 2 generations on · 3 of its ownK243214 Dexcom G7 15 Day Continuous Glucose Monitoring SystemDexcom, Inc. · 2025 · Recalled
  11. Descendant · 2 generations on · 1 of its ownK253737 Dexcom G7 Continuous Glucose Monitoring (CGM) System; Dexcom G7 15…Dexcom, Inc. · 2026
  12. Descendant · 3 generations on · 0 of its ownK261402 Dexcom G7 Continuous Glucose Monitoring System;Dexcom G7 15 Day…Dexcom, Inc. · 2026
  13. Descendant · 2 generations on · 0 of its ownK253710 Dexcom G7 Continuous Glucose Monitoring (CGM) System, Dexcom G7 15…Dexcom, Inc. · 2025

Class I recalls in this family

Most influential descendants

Showing 5 of 5 · See all
  • K240902Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2024 · cites it directly4descendants
  • K243214Dexcom G7 15 Day Continuous Glucose Monitoring SystemDexcom, Inc. · 2025 · 2 generations on3descendants
  • K253737Dexcom G7 Continuous Glucose Monitoring (CGM) System; Dexcom G7 15 Day Continuous…Dexcom, Inc. · 2026 · 2 generations on1descendant
  • K261402Dexcom G7 Continuous Glucose Monitoring System;Dexcom G7 15 Day Continuous Glucose…Dexcom, Inc. · 2026 · 3 generations on0descendants
  • K253710Dexcom G7 Continuous Glucose Monitoring (CGM) System, Dexcom G7 15 Day Continuous…Dexcom, Inc. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7DEN170088Dexcom G6 Continuous Glucose Monitoring SystemDexcom, Inc.2018—
−6K182041Dexcom G6 Glucose Program Continuous Glucose Monitoring SystemDexcom, Inc.2018—
−5K191450Dexcom G6 Continuous Glucose Monitoring System, Dexcom G6 Glucose Program…Dexcom, Inc.20192
−4K200876Dexcom G6 Continuous Glucose Monitoring System, Dexcom G6 Glucose Program…Dexcom, Inc.20201
−3K201328Dexcom G6 Continuous Glucose Monitoring (CGM) SystemDexcom, Inc.2021—
−2K213919Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc.2022Class I
−1K231081Dexcom G7 Continuous Glucose Monitoring (CGM) SystemDexcom, Inc.20231
0 (this device)K234133Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc.2024—
+1K240902Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc.20243
+2K243214Dexcom G7 15 Day Continuous Glucose Monitoring SystemDexcom, Inc.20252
+2K253737Dexcom G7 Continuous Glucose Monitoring (CGM) System; Dexcom G7 15 Day…Dexcom, Inc.2026—
+3K261402Dexcom G7 Continuous Glucose Monitoring System;Dexcom G7 15 Day Continuous…Dexcom, Inc.2026—
+2K253710Dexcom G7 Continuous Glucose Monitoring (CGM) System, Dexcom G7 15 Day…Dexcom, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201810
201910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
202520
202620
FIG. 1 — Lineage of K234133, 2018–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
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
*K231081Dexcom G7 Continuous Glucose Monitoring (CGM) System
Summary page 4
…21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K231081 Dexcom G7 Continuous Glucose Monitoring System…
Dexcom, Inc.20231

Also cleared against K231081: 1 other device →

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K240902Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc.20244

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.

  • K213919Dexcom G7 Continuous Glucose Monitoring SystemDexcom, Inc. · 2022 · 2 generations back · ◆ on the line of descent in FIG. 14 Class I recalls

What does this lineage say?

  • The line of descent spans 6 years and passes through 1 company; a new generation was cleared every 8 months on median.
  • 4 of the 9 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K240902 (Dexcom, Inc., 2024) has gone furthest, with 4 descendants of its own.
  • 1 other device also cites its predicate K231081.

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. 2024, 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 System (Dexcom G7 CGM System or G7) 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…

Read the full statement (139 words)

The Dexcom G7 Continuous Glucose Monitoring System (Dexcom G7 CGM System or G7) 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 purpose of managing diabetes.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K234133: Dexcom G7 Continuous Glucose Monitoring System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K234133

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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