American Laser Medical
Country not established
- Devices
- 5
What American Laser Medical makes
American Laser Medical makes laser systems for medical use, including the Nuvo-Lase 660 Laser System, Nuvolase 720 System for Ophthalmology Laser, Nuvolase 660 Laser System for Ophthalmology, Nuvolase 532 Cutaneous Laser System, and Flex-Lase 600 Series Ion Laser System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Nuvo-Lase 660 Laser System Ref K970667
Regimes: 510(k) Registry: 510(k)Nuvolase 720 System For Ophthalmology Laser Ref K972765
Regimes: 510(k) Registry: 510(k)Nuvolase 660 Laser System For Ophthalmology Ref K972561
Regimes: 510(k) Registry: 510(k)Nuvolase 532 Cutaneous Laser System Ref K990780
Regimes: 510(k) Registry: 510(k)Flex-Lase 600 Series Ion Laser System Ref K963389
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Laser Medical have in the registry?
The registry currently lists 5 devices for American Laser Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Laser Medical's devices?
Among its 5 most recently registered devices, American Laser Medical has devices listed in FDA 510(k) (5 devices).
What risk classes do American Laser Medical's devices fall under?
Among its 5 most recently registered devices, the classes recorded for American Laser Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Laser Medical in the registry?
The most recently registered devices listed for American Laser Medical include NUVO-LASE 660 LASER SYSTEM, NUVOLASE 720 SYSTEM FOR OPHTHALMOLOGY LASER, NUVOLASE 660 LASER SYSTEM FOR OPHTHALMOLOGY and NUVOLASE 532 CUTANEOUS LASER SYSTEM.