Matelaser, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Matelaser, Inc. has 2 FDA 510(k) cleared medical devices. Based in Miami, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Matelaser, Inc. Filter by specialty or product code using the sidebar.
2 devices