510(k) Report

510(k) · Cleared

Cleared

Mallya Injection Pen Adapter (Mallya® for Solostar®)

K222689510(k) TraditionalCleared Dec 5, 202290-day reviewClass II21 CFR 880.5860

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

Biocorp Production · QOG Injection Data Capture Device

Cleared on Dec 5, 2022 as substantially equivalent to K160629 (Companion Medical, Inc., 2016) after a 90-day review. Its family tree reaches back 8 generations to 2001. 4 later devices descend from it.

Decided
Dec 5, 2022
Review
90 days
Class
Class II
Product code
QOG
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K010362 (2001). 16 ancestors in all. 4 later devices descend from it, 2 citing it directly.

  1. Root · 8 generations backK010362 Accu-Chek Comfort Curve Test StripRoche Diagnostics Corp. · 2001 · Recalled
  2. 7 generations backK043474 Accu-Chek Aviva SystemRoche Diagnostics Corp. · 2005 · Recalled
  3. 6 generations backK060620 Accu-Chek Aviva Test StripsRoche Diagnostics Corp. · 2006 · Recalled
  4. 5 generations backK101299 Accu-Chek Aviva Plus Blood Glucose Monitoring SystemRoche Diagnostics · 2011
  5. 4 generations backK111353 Accu-Check Combo SystemRoche Diagnostics · 2012 · Recalled
  6. 3 generations backK141929 Accu-Chek Connect Diabetes Management AppRoche Diagnostics Corporation · 2015 · Recalled
  7. 2 generations backK150910 ACCU-CHEK Connect Diabetes Management AppRoche Diabetes Care, Inc. · 2015 · Recalled
  8. 1 generation backK160629 InPenCompanion Medical, Inc. · 2016 · Recalled
  9. This deviceK222689 Mallya Injection Pen Adapter (Mallya® for Solostar®)Biocorp Production · 2022
  10. Descendant · cites it directly · 2 of its ownK231820 SoloSmart Injection Pen Adapter (SoloSmart®)Biocorp Production · 2024
  11. Descendant · 2 generations on · 1 of its ownK250555 MallyaD injection pen adapter (MallyaD)Biocorp Production · 2025
  12. Descendant · cites it directly · 0 of its ownK243901 SmartPilot YpsoMate NS-A2.25Ypsomed AG · 2025
  13. Descendant · 3 generations on · 0 of its ownK251500 MallyaG Injection Pen Adapter (MallyaG)Biocorp Production · 2025

Most influential descendants

Showing 4 of 4 · See all
  • K231820SoloSmart Injection Pen Adapter (SoloSmart®)Biocorp Production · 2024 · cites it directly2descendants
  • K250555MallyaD injection pen adapter (MallyaD)Biocorp Production · 2025 · 2 generations on1descendant
  • K243901SmartPilot YpsoMate NS-A2.25Ypsomed AG · 2025 · cites it directly0descendants
  • K251500MallyaG Injection Pen Adapter (MallyaG)Biocorp Production · 2025 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K010362Accu-Chek Comfort Curve Test StripRoche Diagnostics Corp.20016
−7K043474Accu-Chek Aviva SystemRoche Diagnostics Corp.200510
−6K060620Accu-Chek Aviva Test StripsRoche Diagnostics Corp.20061
−5K101299Accu-Chek Aviva Plus Blood Glucose Monitoring SystemRoche Diagnostics2011—
−4K111353Accu-Check Combo SystemRoche Diagnostics20123
−3K141929Accu-Chek Connect Diabetes Management AppRoche Diagnostics Corporation20151
−2K150910ACCU-CHEK Connect Diabetes Management AppRoche Diabetes Care, Inc.20156
−1K160629InPenCompanion Medical, Inc.20161
0 (this device)K222689Mallya Injection Pen Adapter (Mallya® for Solostar®)Biocorp Production2022—
+1K231820SoloSmart Injection Pen Adapter (SoloSmart®)Biocorp Production2024—
+2K250555MallyaD injection pen adapter (MallyaD)Biocorp Production2025—
+1K243901SmartPilot YpsoMate NS-A2.25Ypsomed AG2025—
+3K251500MallyaG Injection Pen Adapter (MallyaG)Biocorp Production2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110
200330
200510
200610
200810
201310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
202530
FIG. 1 — Lineage of K222689, 2001–2025Source: 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.

Planning a device in QOG? 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 QOG device

  1. #1 K250555 MallyaD injection pen adapter (MallyaD)score 14.8 · 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
*K160629InPen
Summary page 4
…21 CFR 880.5860 Product Code: QOG 6. Predicate Device: K160629, Companion Medical, InPen 7. Manufacturing Site: Biocorp Production…
Companion Medical, Inc.20161

Also cleared against K160629: 4 other devices →

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K231820SoloSmart Injection Pen Adapter (SoloSmart®)Biocorp Production20242
K243901SmartPilot YpsoMate NS-A2.25Ypsomed AG20250

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 21 years and passes through 6 companies; a new generation was cleared every 2.7 years on median.
  • 12 of the 16 ancestors have a recall of any class.
  • Of its descendants, K231820 (Biocorp Production, 2024) has gone furthest, with 2 descendants of its own.
  • 4 other devices also cite its predicate K160629.

How does its category compare?

All QOG devices

QOG Injection Data Capture Device: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · QOG

3in 2025

2022: 22024: 22025: 3
2007high 3 (2025) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QOG

30in 2025

2025: 30 days median
2007high 30 (2025)2026

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

Recalls per year · QOG

No recall names QOG since 2007.

Adverse event reports per year · QOG

1in 2022

2022: 1
2007high 1 (2022) · low 0 (2007)2025

MAUDE reports naming product code QOG, 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
20190—00
20200—00
20210—00
20222—01
20230—00
20242—00
202533000
20260—0—

What is it indicated for?

The Mallya Injection Pen Adapter is indicated for the capture and wireless transmission of dosing information from compatible reusable and disposable pen injectors. The following Injection pens are compatible.

Mallya designed for Solostar® SANOFI injection pen: Lantus, Toujeo, Admelog, Apidra, and Soliqua 100/33.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K222689: Mallya Injection Pen Adapter (Mallya® for Solostar®).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K222689

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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