510(k) Report

510(k) · Cleared

Cleared

Rightest Blood Glucose Monitoring System GM700

K110737510(k) TraditionalCleared Mar 29, 2012379-day reviewClass II21 CFR 862.1345

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

Bionime Corporation · NBW System, Test, Blood Glucose, Over The Counter

Cleared on Mar 29, 2012 as substantially equivalent to K092052 (Bionime Corporation, 2010) after a 379-day review. Its family tree reaches back 5 generations to 2003. 4 later devices descend from it.

Decided
Mar 29, 2012
Review
379 days
Class
Class II
Product code
NBW
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K024194 (2003). 4 later devices descend from it, 4 citing it directly.

  1. Root · 5 generations backK024194 One Touch Ultra and One Touch Induo Blood Glucose Monitoring SystemsLifescan, Inc. · 2003 · Recalled
  2. 4 generations backK042678 Rightest Blood Glucose Monitoring SystemBionime Corporation · 2005 · Recalled
  3. 3 generations backK053635 Modification to Rightest Blood Glucose Monitoring SystemBionime Corporation · 2006 · Recalled
  4. 2 generations backK062567 Rightest Blood Glucose Monitoring SystemBionime Corporation · 2007 · Recalled
  5. 1 generation backK092052 Rightest Blood Glucose Monitoring System, Model GM550Bionime Corporation · 2010
  6. This deviceK110737 Rightest Blood Glucose Monitoring System GM700Bionime Corporation · 2012
  7. Descendant · cites it directly · 2 of its ownK123008 Rightest Blood Glucose Monitoring System GM700 GE GE200 Blood…Bionime Corporation · 2013
  8. Descendant · cites it directly · 0 of its ownK141292 Rightest Blood Glucose Monitoring System GM700, Rightest Blood…Bionime Coporation · 2015
  9. Descendant · cites it directly · 0 of its ownK133522 Rightest Diabetes Management Software and Adapter (Existing Cleared…Bionime Coporation · 2014
  10. Descendant · cites it directly · 0 of its ownK133003 Rightest Control SolutionBionime Corporation · 2013

Most influential descendants

Showing 4 of 4 · See all
  • K123008Rightest Blood Glucose Monitoring System GM700 GE GE200 Blood Glucose Monitoring System…Bionime Corporation · 2013 · cites it directly2descendants
  • K141292Rightest Blood Glucose Monitoring System GM700, Rightest Blood Glucose Monitoring System…Bionime Coporation · 2015 · cites it directly0descendants
  • K133522Rightest Diabetes Management Software and Adapter (Existing Cleared K113007),Rightest…Bionime Coporation · 2014 · cites it directly0descendants
  • K133003Rightest Control SolutionBionime Corporation · 2013 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K024194One Touch Ultra and One Touch Induo Blood Glucose Monitoring SystemsLifescan, Inc.20035
−4K042678Rightest Blood Glucose Monitoring SystemBionime Corporation20051
−3K053635Modification to Rightest Blood Glucose Monitoring SystemBionime Corporation20061
−2K062567Rightest Blood Glucose Monitoring SystemBionime Corporation20071
−1K092052Rightest Blood Glucose Monitoring System, Model GM550Bionime Corporation2010—
0 (this device)K110737Rightest Blood Glucose Monitoring System GM700Bionime Corporation2012—
+1K123008Rightest Blood Glucose Monitoring System GM700 GE GE200 Blood Glucose…Bionime Corporation2013—
+1K141292Rightest Blood Glucose Monitoring System GM700, Rightest Blood Glucose…Bionime Coporation2015—
+1K133522Rightest Diabetes Management Software and Adapter (Existing Cleared…Bionime Coporation2014—
+1K133003Rightest Control SolutionBionime Corporation2013—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201320
201410
201510
FIG. 1 — Lineage of K110737, 2003–2015Source: 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 NBW? 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 NBW device

  1. #1 K260545 CONTOUR® PLUS BLUE Blood Glucose Monitoring…score 14.6 · 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
*K092052Rightest Blood Glucose Monitoring System, Model GM550
Summary page 2
…Name: Rightest Blood Glucose Monitoring System Model GM550 Device Company: Bionime Corporation 510(K) Number: K092052. 7. Comparison to Predicate Devices: Specification Companison Item Minimum Sample Voum…
Bionime Corporation2010—

Also cleared against K092052: 2 other devices →

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K123008Rightest Blood Glucose Monitoring System GM700 GE GE200 Blood Glucose Monitoring System…Bionime Corporation20132
K141292Rightest Blood Glucose Monitoring System GM700, Rightest Blood Glucose Monitoring System…Bionime Coporation20150
K133522Rightest Diabetes Management Software and Adapter (Existing Cleared K113007),Rightest…Bionime Coporation20140
K133003Rightest Control SolutionBionime Corporation20130

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 9 years and passes through 2 companies; a new generation was cleared every 1.8 years on median.
  • 4 of the 5 ancestors have a recall of any class.
  • Of its descendants, K123008 (Bionime Corporation, 2013) has gone furthest, with 2 descendants of its own.
  • 2 other devices also cite its predicate K092052.

How does its category compare?

All NBW devices

NBW System, Test, Blood Glucose, Over The Counter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · NBW

2in 2025

2007: 292008: 372009: 382010: 312011: 302012: 302013: 472014: 242015: 322016: 202017: 252018: 192019: 102020: 72021: 72022: 122023: 52024: 72025: 22026 (partial year): 5
2007high 47 (2013) · low 2 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NBW

243in 2024

2007: 85 days median2008: 128 days median2009: 140 days median2010: 132 days median2011: 328 days median2012: 230 days median2013: 167 days median2014: 202 days median2015: 237 days median2016: 233 days median2017: 244 days median2018: 168 days median2019: 127 days median2020: 121 days median2021: 465 days median2022: 410 days median2023: 193 days median2024: 243 days median2026 (partial year): 190 days median
2007high 465 (2021) · low 85 (2007)2026

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

Recalls per year · NBW

1in 2025

2007: 92008: 22009: 52010: 112011: 12012: 12013: 5, 2 Class I2014: 12016: 12019: 142025: 1
2007high 14 (2019) · low 0 (2015)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · NBW

4,745in 2025

2007: 7,9912008: 7,7042009: 10,9632010: 11,6312011: 22,9092012: 23,4492013: 35,4082014: 38,5242015: 62,1112016: 76,6212017: 37,5382018: 16,9112019: 14,4722020: 10,7032021: 9,1982022: 8,1032023: 7,2562024: 6,2202025: 4,745
2007high 76,621 (2016) · low 4,745 (2025)2025

MAUDE reports naming product code NBW, 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
2007298597,991
20083712827,704
200938140510,963
2010311321111,631
201130328122,909
201230230123,449
2013471675 (2)35,408
201424202138,524
201532237062,111
201620233176,621
201725244037,538
201819168016,911
2019101271414,472
20207121010,703
2021746509,198
20221241008,103
2023519307,256
2024724306,220
20252—14,745
202651900—

What is it indicated for?

The Rightest Blood Glucose Monitoring System GM700 is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole samples drawn from the fingertips, palm and forearm. The Rightest Blood Glucose Monitoring System GM700 is intended to be used by a single person and should not be shared. The Rightest Blood Glucose Monitoring System GM700 is intended for self testing outside the body (in vitro diagnostic use) by people…

Read the full statement (204 words)

The Rightest Blood Glucose Monitoring System GM700 is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole samples drawn from the fingertips, palm and forearm. The Rightest Blood Glucose Monitoring System GM700 is intended to be used by a single person and should not be shared.

The Rightest Blood Glucose Monitoring System GM700 is intended for self testing outside the body (in vitro diagnostic use) by people with diabetes at home as an aid to monitor the effectiveness of diabetes control. The Rightest Blood Glucose Monitoring System GM700 should not be used for the diagnosis of, or screening for diabetes or for neonatal use. Alternative site testing should be done only during steady - state times (when glucose is not changing rapidly).*

The Rightest Blood Glucose Test Strip GS700 is for use with the Rightest Blood Glucose meter GM700 to quantitatively measure glucose (sugar) in fresh capillary whole blood samples drawn from the fingertip, palm or forearm.

The Rightest Control Solution GC700 is for use with the Rightest Blood Glucose meter GM700 and Rightest Blood Glucose Test Strips GS700 to check that the meters and test strip are working together properly and that the test is performing correctly.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K110737: Rightest Blood Glucose Monitoring System GM700.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K110737

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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