Light Instrument, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Light Instrument, Ltd. makes
Light Instrument, Ltd. makes the Litetouch Dental Laser System, a device used for dental procedures involving soft tissue and hard tissue applications.
The Litetouch Dental Laser 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
Litetouch Dental Laser System Ref K061966
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Light Instrument, Ltd. have in the registry?
The registry currently lists 1 device for Light Instrument, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Light Instrument, Ltd.'s devices?
Among its 1 most recently registered device, Light Instrument, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Light Instrument, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Light Instrument, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Light Instrument, Ltd. in the registry?
The most recently registered devices listed for Light Instrument, Ltd. include LITETOUCH DENTAL LASER SYSTEM.