Luxar Corp.
United StatesFDA applicant, unverified
- Devices
- 17
What Luxar Corp. makes
Luxar Corp. manufactures CO₂ laser systems and associated waveguides, including the LX-20 series and modified versions, designed for surgical precision. Their product line includes rigid and flexible hollow fiber guides (e.g., FlexiGuide™) and endoguiding devices (e.g., EndoGuide®, MicroGuide™) for internal tissue procedures. Applications span podiatry, dermatology, and plastic surgery, with specialized adaptations for endoscopic use. The company also offers modified versions of its original laser systems and endoguiding tools for targeted medical interventions.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Products are listed in the FDA’s 510(k) registry, reflecting their compliance with U.S. medical device authorization requirements. Luxar Corp. is headquartered in the United States.
Catalogue
Search and filter all 17 devicesFrequently asked questions
How many devices does Luxar Corp. have in the registry?
The registry currently lists 17 devices for Luxar Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luxar Corp.'s devices?
Among its 17 most recently registered devices, Luxar Corp. has devices listed in FDA 510(k) (17 devices).
What risk classes do Luxar Corp.'s devices fall under?
Among its 17 most recently registered devices, the classes recorded for Luxar Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Luxar Corp. in the registry?
The most recently registered devices listed for Luxar Corp. include MODIFIED ENDOGUIDE, ENDOGUIDE (R), MICROGUIDE (TM), FLEXIGUIDE (TM), LUXAR MODEL LX-20 MINILASE CO2 LASER and LUXAR MODEL LX-20 CO2 LASER.