Cleartooth Electronics, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3008313821
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
What Cleartooth Electronics, Inc. makes
ClearTooth Electronics, Inc. makes the ClearTooth Digital X-Ray System.
The ClearTooth Digital X-Ray System is a Class II medical device listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Registry: GUDID
Cleartooth Digital X-Ray System Ref K033147
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008313821
- Address
- 106 Mineola Ct., Boulder, CO, 80303
Frequently asked questions
How many devices does CLEARTOOTH ELECTRONICS, INC. have in the registry?
The registry currently lists 2 devices for CLEARTOOTH ELECTRONICS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list CLEARTOOTH ELECTRONICS, INC.'s devices?
Among its 2 most recently registered devices, CLEARTOOTH ELECTRONICS, 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 CLEARTOOTH ELECTRONICS, INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for CLEARTOOTH ELECTRONICS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CLEARTOOTH ELECTRONICS, INC. in the registry?
The most recently registered devices listed for CLEARTOOTH ELECTRONICS, INC. include Cleartooth Digital X-Ray CTDXS and CLEARTOOTH DIGITAL X-RAY SYSTEM.