Light Force Therapy, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Light Force Therapy, Inc. makes
Light Force Therapy, Inc. makes Class II medical devices including SUPER NOVA, ACUBEAM, and DIO.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
Super Nova, Acubeam Ref K001179
Regimes: 510(k) Registry: 510(k)Acubeam, Super Nova, Dio Ref K022888
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Light Force Therapy, Inc. have in the registry?
The registry currently lists 2 devices for Light Force Therapy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Light Force Therapy, Inc.'s devices?
Among its 2 most recently registered devices, Light Force Therapy, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Light Force Therapy, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Light Force Therapy, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Light Force Therapy, Inc. in the registry?
The most recently registered devices listed for Light Force Therapy, Inc. include SUPER NOVA, ACUBEAM and ACUBEAM, SUPER NOVA, DIO.