510(k) · Cleared
ClearedFemale IC (Not Finalized)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Hollister Incorporated · EZD Catheter, Straight
Cleared on Sep 13, 2022 as substantially equivalent to K191633 (Hollister Incorporated, 2019) after a 307-day review. Its family tree reaches back 8 generations to 1991.
- Decided
- Sep 13, 2022
- Review
- 307 days
- Class
- Class II
- Product code
- EZD
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 8 generations to K910022 (1991). 16 ancestors in all, the oldest K896750 (1990). No later device cites it as a predicate yet.
- Root · 8 generations backK910022 MMG/O'neil Urinary Catheterization System KitMedical Marketing Group · 1991
- 7 generations backK973070 Conveen Easicath SetColoplast Corp. · 1997
- 6 generations backK023254 SpeedicathColoplast Corp. · 2003
- 5 generations backK090960 Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142…Hollister, Inc. · 2009
- 4 generations backK110862 Vapro Plus Intermittent CatheterHollister Incorporated · 2011
- 3 generations backK141642 Vapro Intermittent CatheterHollister Incorporated · 2014
- 2 generations backK163179 Onli Intermittent CatheterHollister Incorporated · 2017
- 1 generation backK191633 Infyna ChicHollister Incorporated · 2019
- This deviceK213575 Female IC (Not Finalized)Hollister Incorporated · 2022
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −8 | K910022 | MMG/O'neil Urinary Catheterization System Kit | Medical Marketing Group | 1991 | — |
| −7 | K973070 | Conveen Easicath Set | Coloplast Corp. | 1997 | — |
| −6 | K023254 | Speedicath | Coloplast Corp. | 2003 | — |
| −5 | K090960 | Vapro Intermittent Catheter, Model 72062, 72082,72102, 72122, 72142, 72064… | Hollister, Inc. | 2009 | — |
| −4 | K110862 | Vapro Plus Intermittent Catheter | Hollister Incorporated | 2011 | — |
| −3 | K141642 | Vapro Intermittent Catheter | Hollister Incorporated | 2014 | — |
| −2 | K163179 | Onli Intermittent Catheter | Hollister Incorporated | 2017 | — |
| −1 | K191633 | Infyna Chic | Hollister Incorporated | 2019 | — |
| 0 (this device) | K213575 | Female IC (Not Finalized) | Hollister Incorporated | 2022 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1990 | 1 | 0 |
| 1998 | 1 | 0 |
| 2001 | 4 | 0 |
| 2002 | 1 | 0 |
| 2005 | 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 EZD? 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 EZD device
- #1 K241210 Luja Coudescore 16.2 · 7 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K191633 | Infyna ChicSummary page 4…Product Code/Class: EZD/Class II Classification Name: Catheter, Straight Regulation Number: 21 CFR 876.5130 Predicate Device: Infyna Chic K191633 by Hollister Incorporated. The predicate has not been subject to a design-related recall. Indications for Use: This intermitte… | 2019 |
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 31 years and passes through 4 companies; a new generation was cleared every 3.3 years on median.
- 1 of the 16 ancestors has a recall of any class.
How does its category compare?
All EZD devicesEZD Catheter, Straight: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.
FDA decisions per year · EZD
11so far in 2026, the most since 2007
2026 to Oct 25, outlined.
Median 510(k) review, days · EZD
130in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · EZD
1in 2014
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · EZD
288in 2025
MAUDE reports naming product code EZD, 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 | 4 | 121 | 0 | 0 |
| 2008 | 1 | — | 0 | 0 |
| 2009 | 2 | — | 0 | 4 |
| 2010 | 2 | — | 0 | 6 |
| 2011 | 4 | 116 | 1 | 4 |
| 2012 | 2 | — | 1 | 2 |
| 2013 | 4 | 110 | 0 | 18 |
| 2014 | 5 | 91 | 1 | 17 |
| 2015 | 1 | — | 0 | 21 |
| 2016 | 3 | 83 | 0 | 21 |
| 2017 | 2 | — | 0 | 120 |
| 2018 | 3 | 122 | 0 | 390 |
| 2019 | 0 | — | 0 | 466 |
| 2020 | 1 | — | 0 | 563 |
| 2021 | 0 | — | 0 | 994 |
| 2022 | 10 | 288 | 0 | 487 |
| 2023 | 6 | 214 | 0 | 553 |
| 2024 | 5 | 147 | 0 | 116 |
| 2025 | 6 | 130 | 0 | 288 |
| 2026 | 11 | 146 | 0 | — |
What is it indicated for?
This intermittent catheter is a flexible tubular device that is inserted through the urethra by female and female pediatric patients who need to drain urine from the bladder.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K213575 · printed Nov 6, 2026
Cite this page
510(k) Report. “K213575: Female IC (Not Finalized).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K213575
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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