American Laser Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What American Laser Corp. makes
American Laser Corp. manufactures laser photocoagulation devices, including argon medical lasers and integrated laser delivery systems for ophthalmic applications. Their portfolio includes the Nuvolase 532 laser system, designed for precise tissue treatment in medical procedures. These devices are used primarily in retinal surgeries and other laser-based medical interventions.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. Their products are intended for use within the United States, adhering to FDA compliance standards for laser-based medical instruments.
Catalogue
Laser Photocoagulator Argon Med. Laser Ref K813429
Regimes: 510(k) Registry: 510(k)Laser Photocoagulator Ref K827819
Regimes: 510(k) Registry: 510(k)Bq/Bm Integrated Laser Delivery System Ref K990665
Regimes: 510(k) Registry: 510(k)Nuvolase 532 Laser System Ref K990725
Regimes: 510(k) Registry: 510(k)Nuvolase 532 Medical Laser System Ref K010046
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Laser Corp. have in the registry?
The registry currently lists 5 devices for American Laser Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Laser Corp.'s devices?
Among its 5 most recently registered devices, American Laser Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do American Laser Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for American Laser Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Laser Corp. in the registry?
The most recently registered devices listed for American Laser Corp. include LASER PHOTOCOAGULATOR ARGON MED. LASER, LASER PHOTOCOAGULATOR, BQ/BM INTEGRATED LASER DELIVERY SYSTEM and NUVOLASE 532 LASER SYSTEM.