Photo Therapeutics, Inc.
Country not established
- Devices
- 7
What Photo Therapeutics, Inc. makes
Photo Therapeutics, Inc. manufactures ultraviolet (UV) devices for medical use, including the OMNILUX NEW-U and OMNILUX CLEAR-U systems. These devices are designed for phototherapy applications, such as treating skin conditions like psoriasis and vitiligo, using controlled UV light exposure.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. The devices are listed in the FDA’s regulatory database, and the company is based in the United States.
Catalogue
Omnilux New-U Ref K072459
Regimes: 510(k) Registry: 510(k)Omnilux Revive And Blue Ref K043329
Regimes: 510(k) Registry: 510(k)Omnilux Plus Ref K043317
Regimes: 510(k) Registry: 510(k)Omnilux Blue Ref K030883
Regimes: 510(k) Registry: 510(k)Omnilux Revive And Omnilux Plus Ref K050216
Regimes: 510(k) Registry: 510(k)Omnilux Red Ref K030426
Regimes: 510(k) Registry: 510(k)Omnilux Clear-U Ref K081307
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Photo Therapeutics, Inc. have in the registry?
The registry currently lists 7 devices for Photo Therapeutics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Photo Therapeutics, Inc.'s devices?
Among its 7 most recently registered devices, Photo Therapeutics, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Photo Therapeutics, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Photo Therapeutics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Photo Therapeutics, Inc. in the registry?
The most recently registered devices listed for Photo Therapeutics, Inc. include OMNILUX NEW-U, OMNILUX REVIVE AND BLUE, OMNILUX PLUS and OMNILUX BLUE.