Endophotonix, Inc.
Country not established
- Devices
- 1
What Endophotonix, Inc. makes
Endophotonix, Inc. manufactures laser ablation systems designed for precise tissue removal or modification, including models like the LU-1083-25, LF-1083, and PC-1000. These devices are intended for medical procedures requiring controlled laser energy, such as dermatological treatments or surgical applications.
The company’s laser ablation systems fall under FDA Class II devices and are listed via the 510(k) pathway. These products are regulated under US medical device laws and are based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endophotonix, Inc. have in the registry?
The registry currently lists 1 device for Endophotonix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endophotonix, Inc.'s devices?
Among its 1 most recently registered device, Endophotonix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Endophotonix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Endophotonix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endophotonix, Inc. in the registry?
The most recently registered devices listed for Endophotonix, Inc. include SOLAR LASER ABLATION SYSTEM, MODELS: LU-1083-25, LF-1083, PC-1000, IC-1083, LW-2000, LG-2001, LK-001, PM-1083, TF-1083.