Curae'Lase, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Curae'Lase, Inc. makes
Curae'Lase, Inc. manufactures infrared (IR) laser systems and laser modules, including the CURAE'LASE CL1000 IR LASER SYSTEM and the CL10009 IR LASER, designed for medical applications requiring precise laser delivery.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Curae'lase CL1000 Ir Laser System Ref K053201
510(k) 510(k)CL10009 Ir Laser Ref K130168
510(k) 510(k)
Frequently asked questions
How many devices does Curae'Lase, Inc. have in the registry?
The registry currently lists 2 devices for Curae'Lase, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Curae'Lase, Inc.'s devices?
Among its 2 most recently registered devices, Curae'Lase, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Curae'Lase, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Curae'Lase, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Curae'Lase, Inc. in the registry?
The most recently registered devices listed for Curae'Lase, Inc. include CURAE'LASE CL1000 IR LASER SYSTEM and CL10009 IR LASER.