MateLaser Medical Diode Laser Systems (ML-DLS-30)— 510(k) K250731
Substantially EquivalentMatelaser, Inc.
FDA 510(k) clearance K250731 for MateLaser Medical Diode Laser Systems (ML-DLS-30), Substantially Equivalent on 2025-10-16. Applicant: Matelaser, Inc.. Device class: 2.
Clearance details
- Applicant
- Matelaser, Inc.
- Product code
- Code NVK
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
Recent devices under product code NVK
view allMore clearances from Matelaser, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.