Aesculight, LLC
Country not established
- Devices
- 1
What Aesculight, LLC makes
Aesculight, LLC manufactures flexible fibers, handpieces, and tips designed for use with CO₂ surgical lasers. These components are intended to facilitate precise laser delivery in surgical procedures, supporting applications in dermatology, ophthalmology, and other medical specialties.
The company’s products fall under FDA Class II devices and are listed via the 510(k) pathway. The portfolio is regulated under US medical device regulations, with no additional international registries specified. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aesculight, LLC have in the registry?
The registry currently lists 1 device for Aesculight, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aesculight, LLC's devices?
Among its 1 most recently registered device, Aesculight, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Aesculight, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Aesculight, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aesculight, LLC in the registry?
The most recently registered devices listed for Aesculight, LLC include AESCULIGHT FAMILY OF FLEXIBLE FIBERS, HANDPIECES AND TIPS FOR CO2 SURGICAL LASERS.