Collagen Wound Powder— 510(k) K260596

Name: FDA 510(k) clearance K260596
Creator: U.S. Food and Drug Administration
Published: 2026-07-02

Substantially Equivalent

Ventris Medical

FDA 510(k) clearance K260596 for Collagen Wound Powder, Substantially Equivalent on 2026-07-02. Applicant: Ventris Medical. Device class: Unclassified.

Clearance details

Applicant: Ventris Medical
Product code: Code KGN
Device class: Unclassified
Advisory panel: Unknown
Date received: 2026-02-24
Decision date: 2026-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newport Beach, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KGN

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K260711 — Accelagen Plus Surgical Matrix, 1cc (CG-01AP) +4 more2026-08-27
K260669 — Endoform Dermal Template2026-06-24
K253521 — ECMT-100 WMD2026-06-18
K253204 — Catalyze2026-06-05
K253974 — Roosin Collagen Dressing2026-06-03

More clearances from Ventris Medical

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K250556 — Porous Biologic Scaffold2025-03-21
K240765 — Porous Biologic Scaffold2024-12-18
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K221644 — Synthetic Bone Putty2022-09-02

Adverse events under product code KGN

product code KGN

Other: 2
Total: 2

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.