Klox Technlogies, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Klox Technlogies, Inc. makes
Klox Technologies, Inc. makes the Klox Biophotonic LumiHeal System, a biophotonic device intended for therapeutic light-based treatment.
The Klox Biophotonic LumiHeal System is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Klox Biophotonic LumiHeal System Ref DEN200005
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Klox Technlogies, Inc. have in the registry?
The registry currently lists 1 device for Klox Technlogies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Klox Technlogies, Inc.'s devices?
Among its 1 most recently registered device, Klox Technlogies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Klox Technlogies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Klox Technlogies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Klox Technlogies, Inc. in the registry?
The most recently registered devices listed for Klox Technlogies, Inc. include Klox Biophotonic LumiHeal System.