Livermoretech, Inc
United Statesfrom the FDA registration address FDA establishment FEI 3014209556
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
EZER, Portable X-ray System Ref K193535
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
LaVid FMTS DIAGNOSTIC X-RAY SYSTEM Ref K180663
Regimes: 510(k) Registry: 510(k)E-Com Dr-2000 Dr Ref K193644
Regimes: 510(k) Registry: 510(k)EZER, Portable X-ray System Ref K190935
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3014209556
- Address
- 801 north Jupiter rd suite 200, Plano, TX, 75074
Frequently asked questions
How many devices does LIVERMORETECH,INC have in the registry?
The registry currently lists 9 devices for LIVERMORETECH,INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list LIVERMORETECH,INC's devices?
Among its 9 most recently registered devices, LIVERMORETECH,INC has devices listed in FDA 510(k) (6 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do LIVERMORETECH,INC's devices fall under?
Among its 9 most recently registered devices, the classes recorded for LIVERMORETECH,INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LIVERMORETECH,INC in the registry?
The most recently registered devices listed for LIVERMORETECH,INC include AirTouch AirTouch 905, AirTouch, EZER, EUROPA AirTouch 602, AirTouch AirTouch 855 and EZER, Portable X-ray System.