Live Medica, LLC
United Statesfrom the FDA registration address FDA FEI 3048085746
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
LiveMedica Enterprise PACS Ref K253927
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3048085746
- DUNS number
- 145271075
- Address
- 11552 Auldbury Way, Raleigh, NC, 27617
Frequently asked questions
How many devices does Live Medica, LLC have in the registry?
The registry currently lists 2 devices for Live Medica, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Live Medica, LLC's devices?
Among its 2 most recently registered devices, Live Medica, LLC 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 Live Medica, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Live Medica, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Live Medica, LLC in the registry?
The most recently registered devices listed for Live Medica, LLC include Live Medica Enterprise PACS 2 and LiveMedica Enterprise PACS.