Guidemia Technologies, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3013634985
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
What Guidemia Technologies, LLC makes
Guidemia Technologies, LLC manufactures the Guidemia and GuideMia Ortho+ software systems. These products are specialized medical imaging and planning software applications.
The company is based in the United States. Its devices are classified as Class II medical devices and are listed in the FDA 510(k) regulatory registry.
Catalogue
Guidemia Ref K121466
Regimes: 510(k) Registry: 510(k)GuideMia Ortho+ Ref K162850
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3013634985
- Address
- 6532 University Way, Buena Park, CA, 90620
Frequently asked questions
How many devices does GUIDEMIA TECHNOLOGIES, LLC have in the registry?
The registry currently lists 2 devices for GUIDEMIA TECHNOLOGIES, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list GUIDEMIA TECHNOLOGIES, LLC's devices?
Among its 2 most recently registered devices, GUIDEMIA TECHNOLOGIES, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do GUIDEMIA TECHNOLOGIES, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for GUIDEMIA TECHNOLOGIES, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from GUIDEMIA TECHNOLOGIES, LLC in the registry?
The most recently registered devices listed for GUIDEMIA TECHNOLOGIES, LLC include GUIDEMIA and GuideMia Ortho+.