Lumen Development and Manufacturing, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TWINWAVE DENTAL LASER, TIDALWAVE 810 DENTAL LASER, TIDALWAVE 980 DENTAL LASER
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Lumen Development and Manufacturing, Inc. General & Plastic Surgery ✕
1 devices