Lumenis, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: AcuPulse CO2 Laser System, Delivery Devices and Accessories, UltraPulse Surgical and Aesthetic CO2 Laser System, Delivery Devices and Accessories, AcuPulse W CO2 Laser Systems, Delivery Devices and Accessories
28
Total
27
Cleared
1
Denied
FDA 510(k) Regulatory Record - Lumenis, Ltd. Ophthalmic ✕
1 devices