C. Light Technologies, Inc.
Country not established FDA FEI 3027593072
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- GUDID
Retitrack Ref K222484
510(k) 510(k)
Company details
- FDA FEI number
- 3027593072
- DUNS number
- 079570312
- Address
- 1700 Wyatt Dr., Santa Clara, CA, 95054
- [email protected]
- Phone
- +1(999)999-9999
Frequently asked questions
How many devices does C. Light Technologies, Inc. have in the registry?
The registry currently lists 2 devices for C. Light Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list C. Light Technologies, Inc.'s devices?
Among its 2 most recently registered devices, C. Light Technologies, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do C. Light Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for C. Light Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from C. Light Technologies, Inc. in the registry?
The most recently registered devices listed for C. Light Technologies, Inc. include Retitrack CR1 and Retitrack.