K250731
- 510(k) number
- K250731
- Device name
- MateLaser Medical Diode Laser Systems (ML-DLS-30)
- Applicant
- Matelaser, Inc. FL · US
- Product code
- NVK — Laser, Dental, Soft Tissue
- Decision date
- 2025-10-16
- Date received
- 2025-03-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K250731.pdf
Official FDA record: K250731
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.