K252673
- 510(k) number
- K252673
- Device name
- LacertaMatrix
- Applicant
- Lacerta Life Science LA · US
- Product code
- KGN — Wound Dressing With Animal-Derived Material(S)
- Decision date
- 2025-12-22
- Date received
- 2025-08-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K252673.pdf
Official FDA record: K252673
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.