K260020
- 510(k) number
- K260020
- Device name
- Redermo Wound Matrix
- Applicant
- Beijing Kreate Medical Co., Ltd. CN
- Product code
- QSZ — Absorbable Synthetic Wound Dressing
- Decision date
- 2026-04-16
- Date received
- 2026-01-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K260020.pdf
Official FDA record: K260020
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.