510(k) · Cleared
ClearedPatch, Pledget and Intracardiac
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Cormatrix Cardiovascular, Inc. · DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene
Cleared on Jul 26, 2011 as substantially equivalent to K063349 (Cormatrix Cardiovascular, Inc., 2007) and 3 other predicates after a 90-day review. Its family tree reaches back 6 generations to 1992. 1 later device descends from it.
- Decided
- Jul 26, 2011
- Review
- 90 days
- Class
- Class II
- Product code
- DXZ
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 6 generations to K921895 (1992). 28 ancestors in all, the oldest K830889 (1983). 1 later device descends from it, 1 citing it directly.
- Root · 6 generations backK921895 Tissue Patch, Tissue GraftBio-Vascular, Inc. · 1992
- 5 generations backK961810 Supple Peri-Guard PericardiumBio-Vascular, Inc. · 1996
- 4 generations backK980431 SurgisisCook Biotech, Inc. · 1998
- 3 generations backK020455 Tissuemend Soft Tissue Repair MatrixTei Biosciences, Inc. · 2002
- 2 generations backK051405 Regensis Pericardial PatchCormatrix Cardiovascular, Inc. · 2005
- 1 generation backK063349 Cormatrix Patch for Cardiac Tissue RepairCormatrix Cardiovascular, Inc. · 2007
- This deviceK111187 Patch, Pledget and IntracardiacCormatrix Cardiovascular, Inc. · 2011
- Descendant · cites it directly · 0 of its ownK140789 Cormatrix Ecm for Vascular RepairCormatrix Cardiovascular, Inc. · 2014
Most influential descendants
Showing 1 of 1 · See all- K140789Cormatrix Ecm for Vascular RepairCormatrix Cardiovascular, Inc. · 2014 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K921895 | Tissue Patch, Tissue Graft | Bio-Vascular, Inc. | 1992 | — |
| −5 | K961810 | Supple Peri-Guard Pericardium | Bio-Vascular, Inc. | 1996 | — |
| −4 | K980431 | Surgisis | Cook Biotech, Inc. | 1998 | — |
| −3 | K020455 | Tissuemend Soft Tissue Repair Matrix | Tei Biosciences, Inc. | 2002 | — |
| −2 | K051405 | Regensis Pericardial Patch | Cormatrix Cardiovascular, Inc. | 2005 | — |
| −1 | K063349 | Cormatrix Patch for Cardiac Tissue Repair | Cormatrix Cardiovascular, Inc. | 2007 | — |
| 0 (this device) | K111187 | Patch, Pledget and Intracardiac | Cormatrix Cardiovascular, Inc. | 2011 | — |
| +1 | K140789 | Cormatrix Ecm for Vascular Repair | Cormatrix Cardiovascular, Inc. | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1983 | 1 | 0 |
| 1985 | 1 | 0 |
| 1991 | 1 | 0 |
| 1992 | 1 | 0 |
| 1993 | 1 | 0 |
| 1994 | 1 | 0 |
| 1996 | 2 | 0 |
| 1997 | 2 | 0 |
| 1998 | 5 | 0 |
| 2000 | 2 | 0 |
| 2001 | 1 | 0 |
| 2003 | 1 | 0 |
| 2004 | 2 | 0 |
| 2005 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 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 DXZ? 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 DXZ device
- #1 K240775 PeriBeam® Pericardial Membranescore 9.2 · 1 generation · no Class I recall
- #2 Held for the reportin the report
What was it cleared against? (4)
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 |
|---|---|---|---|
| * | K063349 | Cormatrix Patch for Cardiac Tissue RepairSummary page 2…5 10(k).PRiEiARKEr NOTIFICATION SECTION 5 510(k) SUMMARY (CONT.). PREDICATE DEVICES " CarMatrix® ECM® for Cardiac Tissue Repair (K(063349) " Cook® Biotech Surgisis® Peripheral Vascular Patch (K00 1785) " Bic-Vasedlar/Synovis® Vascu-Guard® Peripheral Vascu… | 2007 |
| * | K001785 | Surgisis Peripheral Vascular PatchSummary page 2…TION 5 510(k) SUMMARY (CONT.). PREDICATE DEVICES " CarMatrix® ECM® for Cardiac Tissue Repair (K(063349) " Cook® Biotech Surgisis® Peripheral Vascular Patch (K00 1785) " Bic-Vasedlar/Synovis® Vascu-Guard® Peripheral Vascular Patch (K(983602) " Carbomedics.Vascute k Thin Wall Carotid… | 2000 |
| * | K983602 | CV Peri-Guard and Vascu-GuardSummary page 2…iac Tissue Repair (K(063349) " Cook® Biotech Surgisis® Peripheral Vascular Patch (K00 1785) " Bic-Vasedlar/Synovis® Vascu-Guard® Peripheral Vascular Patch (K(983602) " Carbomedics.Vascute k Thin Wall Carotid Patch (K(96361 1) INTENDED USE The Co~trx ECM® for Carotid Repair is intended f… | 1998 |
| * | K963611 | Vascutek Cardiovascular Fabric: Vascutek Gelseal Patch,Vascutek Gelsoft Patch,Vascutek… | 1996 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K140789 | Cormatrix Ecm for Vascular Repair | 2014 | 0 |
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 19 years and passes through 4 companies; a new generation was cleared every 3.6 years on median.
- 5 of the 28 ancestors have a recall of any class.
- Of its descendants, K140789 (Cormatrix Cardiovascular, Inc., 2014) has gone furthest, with 0 descendants of its own.
- 4 other devices also cite its predicate K063349.
How does its category compare?
All DXZ devicesDXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · DXZ
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DXZ
106in 2014
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DXZ
2in 2025
Class I (2 since 2007) Class II/III not classified
Adverse event reports per year · DXZ
119in 2025
MAUDE reports naming product code DXZ, 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 | 50 |
| 2008 | 2 | — | 0 | 6 |
| 2009 | 1 | — | 0 | 109 |
| 2010 | 3 | 91 | 2 | 81 |
| 2011 | 2 | — | 2 | 47 |
| 2012 | 1 | — | 0 | 21 |
| 2013 | 1 | — | 2 | 69 |
| 2014 | 3 | 106 | 0 | 93 |
| 2015 | 2 | — | 0 | 171 |
| 2016 | 2 | — | 0 | 66 |
| 2017 | 1 | — | 0 | 30 |
| 2018 | 0 | — | 1 | 44 |
| 2019 | 0 | — | 0 | 55 |
| 2020 | 1 | — | 1 | 121 |
| 2021 | 0 | — | 0 | 80 |
| 2022 | 0 | — | 0 | 77 |
| 2023 | 0 | — | 2 | 40 |
| 2024 | 0 | — | 0 | 49 |
| 2025 | 1 | — | 2 (2) | 119 |
| 2026 | 0 | — | 1 | — |
What is it indicated for?
The CorMatrix® ECM® for Carotid Repair is intended for use as a patch material for vascular reconstruction and repair of the carotid artery, including patch closure following carotid endarterectomy and suture line buttressing.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K111187 · printed Nov 6, 2026
Cite this page
510(k) Report. “K111187: Patch, Pledget and Intracardiac.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111187
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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