510(k) Report

510(k) · Cleared

Cleared

Primatrix Dermal Repair Scaffold

K131286510(k) TraditionalCleared Aug 5, 201391-day reviewClass U

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

Tei Biosciences, Inc. · KGN Wound Dressing With Animal-Derived Material (S)

Cleared on Aug 5, 2013 as substantially equivalent to K083440 (Tei Biosciences, Inc., 2008) and 1 other predicate after a 91-day review. Its family tree reaches back 6 generations to 1988. 5 later devices descend from it.

Decided
Aug 5, 2013
Review
91 days
Class
Class U
Product code
KGN
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K881854 (1988). 12 ancestors in all. 5 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2006: 1 other ancestor1998: 1 other ancestor1993: 1 other ancestor1991: 3 other ancestors2016: 1 descendant cleared2025: 2 descendants cleared2021: 1 descendant cleared2026: 1 descendant clearedK881854 · Sorbsan Topical Wound Dressing · E.G. Dick & Assoc. · 1988K982597 · Fibrcol Plus Collagen Wound Dressing with Alginate · Johnson & Johnson Medical, Inc. · 1998K993948 · Sis Wound Dressing II · Cook Biotech, Inc. · 2000K023778 · Dressskin · Tei Biosciences, Inc. · 2003K061407 · Primatrix Dermal Repair Scaffold · Tei Biosciences, Inc. · 2006K083440 · Primatrix Dermal Repair Scaffold · Tei Biosciences, Inc. · 20081990200020102020
  1. Root · 6 generations backK881854 Sorbsan Topical Wound DressingE.G. Dick & Assoc. · 1988
  2. 5 generations backK982597 Fibrcol Plus Collagen Wound Dressing with AlginateJohnson & Johnson Medical, Inc. · 1998
  3. 4 generations backK993948 Sis Wound Dressing IICook Biotech, Inc. · 2000
  4. 3 generations backK023778 DressskinTei Biosciences, Inc. · 2003
  5. 2 generations backK061407 Primatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2006
  6. 1 generation backK083440 Primatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2008
  7. This deviceK131286 Primatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2013
  8. Descendant · cites it directly · 4 of its ownK153690 PriMatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2016 · Recalled
  9. Descendant · 2 generations on · 2 of its ownK201577 MatriDermMedskin Solutions Dr. Suwelack AG · 2021
  10. Descendant · 3 generations on · 0 of its ownK261224 MatriDermMedskin Solutions Dr. Suwelack AG · 2026
  11. Descendant · 3 generations on · 0 of its ownK250864 MatriDerm pluS+ Bi-LayerMedskin Solutions Dr. Suwelack AG · 2025
  12. Descendant · 2 generations on · 0 of its ownK250397 Helios Dermal ScaffoldHelios Biomedical, Inc. · 2025

Most influential descendants

Showing 5 of 5 · See all
  • K153690PriMatrix Dermal Repair ScaffoldTei Biosciences, Inc. · 2016 · cites it directly4descendants
  • K201577MatriDermMedskin Solutions Dr. Suwelack AG · 2021 · 2 generations on2descendants
  • K261224MatriDermMedskin Solutions Dr. Suwelack AG · 2026 · 3 generations on0descendants
  • K250864MatriDerm pluS+ Bi-LayerMedskin Solutions Dr. Suwelack AG · 2025 · 3 generations on0descendants
  • K250397Helios Dermal ScaffoldHelios Biomedical, Inc. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K881854Sorbsan Topical Wound DressingE.G. Dick & Assoc.1988—
−5K982597Fibrcol Plus Collagen Wound Dressing with AlginateJohnson & Johnson Medical, Inc.1998—
−4K993948Sis Wound Dressing IICook Biotech, Inc.2000—
−3K023778DressskinTei Biosciences, Inc.2003—
−2K061407Primatrix Dermal Repair ScaffoldTei Biosciences, Inc.2006—
−1K083440Primatrix Dermal Repair ScaffoldTei Biosciences, Inc.2008—
0 (this device)K131286Primatrix Dermal Repair ScaffoldTei Biosciences, Inc.2013—
+1K153690PriMatrix Dermal Repair ScaffoldTei Biosciences, Inc.20164
+2K201577MatriDermMedskin Solutions Dr. Suwelack AG2021—
+3K261224MatriDermMedskin Solutions Dr. Suwelack AG2026—
+3K250864MatriDerm pluS+ Bi-LayerMedskin Solutions Dr. Suwelack AG2025—
+2K250397Helios Dermal ScaffoldHelios Biomedical, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199130
199310
199810
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
202110
202520
202610
FIG. 1 — Lineage of K131286, 1988–2026Source: 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 KGN? 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 KGN device

  1. #1 K231325 Corplex P / Theracor P / Allacor Pscore 17.9 · 8 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K083440Primatrix Dermal Repair Scaffold
Summary page 1
…nction and intended use to: IPredicate Devices IManufacturer I 510(k) Number PriMatrix TEI Biosciences IK083440 DressSkin TEI Biosciences IK023778 - 14- ===…
Tei Biosciences, Inc.2008—
*K023778Dressskin
Summary page 1
…I 510(k) Number PriMatrix TEI Biosciences IK083440 DressSkin TEI Biosciences IK023778 - 14- TEX BIOSCIENCES INC. PriMatrix…
Tei Biosciences, Inc.2003—

Also cleared against K083440: 3 other devices →

What descends from it? (5)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K153690PriMatrix Dermal Repair ScaffoldTei Biosciences, Inc.20164

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 25 years and passes through 4 companies; a new generation was cleared every 3.7 years on median.
  • None of the 12 ancestors has a recall.
  • Of its descendants, K153690 (Tei Biosciences, Inc., 2016) has gone furthest, with 4 descendants of its own.
  • 3 other devices also cite its predicate K083440.

How does its category compare?

All KGN devices

KGN Wound Dressing With Animal-Derived Material (S): FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · KGN

15so far in 2026, the most since 2007

2007: 32008: 62009: 82010: 42011: 72012: 82013: 62014: 52015: 72016: 42017: 72018: 62019: 32020: 52021: 62022: 122023: 92024: 132025: 102026 (partial year): 15
2007high 15 (2026) · low 3 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KGN

162in 2025

2007: 32 days median2008: 87 days median2009: 121 days median2010: 175 days median2011: 228 days median2012: 123 days median2013: 147 days median2014: 188 days median2015: 87 days median2016: 164 days median2017: 136 days median2018: 148 days median2019: 128 days median2020: 279 days median2021: 236 days median2022: 246 days median2023: 194 days median2024: 83 days median2025: 162 days median2026 (partial year): 174 days median
2007high 279 (2020) · low 32 (2007)2026

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

Recalls per year · KGN

3in 2018

2017: 12018: 3
2007high 3 (2018) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · KGN

15in 2025

2008: 12009: 22010: 32011: 62012: 42013: 62014: 122015: 92016: 62017: 82018: 152019: 112020: 172021: 142022: 132023: 212024: 152025: 15
2007high 21 (2023) · low 0 (2007)2025

MAUDE reports naming product code KGN, 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
200733200
200868701
2009812102
2010417503
2011722806
2012812304
2013614706
20145188012
201578709
2016416406
2017713618
20186148315
20193128011
20205279017
20216236014
202212246013
20239194021
20241383015
202510162015
2026151740—

What is it indicated for?

PriMatrix is Intended for the management of wounds that include:

* Partial and full thickness wounds

* Pressure, diabetic, and venous ulcers

* Second-degree burns

* Surgical wounds-donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence

* Trauma wounds-abrasions, lacerations, and skin tears

* Tunneled/undermined wounds

* Draining wounds

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K131286: Primatrix Dermal Repair Scaffold.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131286

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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