Azure Microdynamics, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3007279910
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3007279910
- Address
- 19652 Descartes, Foothill Ranch, CA, 92610
Frequently asked questions
How many devices does AZURE MICRODYNAMICS, INC. have in the registry?
The registry currently lists 4 devices for AZURE MICRODYNAMICS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list AZURE MICRODYNAMICS, INC.'s devices?
Among its 4 most recently registered devices, AZURE MICRODYNAMICS, INC. has devices listed in FDA GUDID (4 devices).
What risk classes do AZURE MICRODYNAMICS, INC.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for AZURE MICRODYNAMICS, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from AZURE MICRODYNAMICS, INC. in the registry?
The most recently registered devices listed for AZURE MICRODYNAMICS, INC. include VECS Palate Expander 1005-10, VECS Lab Kit 9005-02, VECS Palate Expander 1005-14 and VECS Activation Key 9005-01.