510(k) · Cleared
ClearedFlexi-Q DV and DVR Auto-Injectors
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Elcam Medical Acal · KZH Introducer, Syringe Needle
Cleared on Feb 9, 2012 as substantially equivalent to K001293 (Medimop Medical Projects, Ltd., 2000) and 1 other predicate after a 259-day review. Its family tree reaches back 2 generations to 1995.
- Decided
- Feb 9, 2012
- Review
- 259 days
- Class
- Class II
- Product code
- KZH
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 2 generations to K945660 (1995). 3 ancestors in all. No later device cites it as a predicate yet.
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K945660 | Autoject 2 | Owen Mumford USA, Inc. | 1995 | 3 |
| −1 | K013362 | Autoject 2 | Owen Mumford USA, Inc. | 2001 | — |
| 0 (this device) | K111467 | Flexi-Q DV and DVR Auto-Injectors | Elcam Medical Acal | 2012 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 1 | 0 |
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 KZH? 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 KZH device
- #1 K243232 GripMatescore 9.4 · 4 generations · no Class I recall
- #2 Held for the reportin the report
What was it cleared against? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K001293 | Modification to Mixject Dispensing Pin/with Detachable Vial Holder/with Detachable Vial…Summary page 2…Mixject Dispensing Pin with Detachable Vial Holder and Pre- attached Needle from Medimop Medical Projects Ltd Ratanana, Israel, cleared under 5 10(k) K001293 and Autoject 2 from Owen Mumford USA Inc, Marietta, GA, USA, cleared under 510(k) K(013362. Device descripti… | 2000 |
| * | K013362 | Autoject 2Summary page 3…Ltd, Ra'anana, Israel, cleared under 510(k) number K001293 and Autoject 2 from Owen Mumford USA Inc, Marietta, GA, USA, cleared under 510(k) number K013362 when used together and is therefore substantially equivalent to the predicate devices. Conclusion:… | 2001 |
What descends from it?
No later submission names this one as a predicate yet.
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 17 years and passes through 2 companies; a new generation was cleared every 10.2 years on median.
- 1 of the 3 ancestors has a recall of any class.
- 6 other devices also cite its predicate K001293.
How does its category compare?
All KZH devicesKZH Introducer, Syringe Needle: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.
FDA decisions per year · KZH
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · KZH
Too few KZH 510(k)s in any year since 2007 to give a median.
Recalls per year · KZH
2in 2019
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KZH
16in 2025
MAUDE reports naming product code KZH, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 1 | — | 0 | 2 |
| 2008 | 2 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 3 |
| 2011 | 0 | — | 1 | 20 |
| 2012 | 2 | — | 0 | 20 |
| 2013 | 1 | — | 0 | 53 |
| 2014 | 1 | — | 0 | 138 |
| 2015 | 0 | — | 0 | 99 |
| 2016 | 1 | — | 0 | 68 |
| 2017 | 1 | — | 0 | 88 |
| 2018 | 0 | — | 0 | 88 |
| 2019 | 0 | — | 2 | 95 |
| 2020 | 0 | — | 0 | 158 |
| 2021 | 0 | — | 0 | 87 |
| 2022 | 1 | — | 0 | 58 |
| 2023 | 0 | — | 0 | 35 |
| 2024 | 1 | — | 0 | 27 |
| 2025 | 0 | — | 0 | 16 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Flexi-Q DV Auto-injector is indicated for the transfer and automated subcutaneous injection of FDA approved drugs and biologics in compatible vials.
The Flexi-Q DV Auto-injector is intended for use in the home environment by the patient or care-giver after training by a Health Care Professional.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K111467 · printed Nov 4, 2026
Cite this page
510(k) Report. “K111467: Flexi-Q DV and DVR Auto-Injectors.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K111467
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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